Variant Details

Variant: esv2668847

Internal ID

9934952

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr9:36474249..36475082	hg38	UCSC Ensembl
	chr9:36474246..36475079	hg19	UCSC Ensembl

Cytoband

9p13.2

Allele length

Assembly	Allele length
hg38	834
hg19	834

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5665632, essv5822281, essv5551188, essv6552637, essv6324599, essv5462159, essv5742803, essv5811969, essv5627657, essv6538353, essv6372007, essv5747717, essv5531155, essv6315372, essv6189113, essv6111274, essv5438978, essv6395520, essv6138680, essv5743505, essv5529261, essv5894604, essv6298071, essv6582886, essv5979588, essv6079436, essv6498919, essv6355916, essv5993580, essv6567241, essv5759597, essv5608312, essv6430787, essv5485110, essv6042452, essv6447144, essv5684471, essv6561179, essv6324350, essv5777970, essv6198525, essv5682571, essv5400761, essv5538538, essv6230982, essv5847893, essv6121532, essv6037731, essv5529787, essv5466066, essv5580530, essv6402611, essv6348164, essv5779413, essv5941927, essv5899423, essv5961360, essv6181733, essv5565645, essv6435120, essv6569751, essv5500489, essv6389632, essv6398571, essv5579393, essv6216878, essv6485533, essv5784859, essv5754246, essv5982845, essv6370781, essv6084349, essv5799633, essv6494336, essv5845446, essv5599595, essv5406820, essv5690939, essv5797774, essv6470082, essv6380480, essv5945381, essv5467993, essv5856692, essv5405651, essv5987290, essv6331731, essv5840280, essv5499348, essv5928752, essv6173084, essv6515234, essv6521968, essv5790615, essv6072083, essv6171902, essv5834405, essv5867610, essv5753835, essv6585359, essv5767284, essv6340619, essv6268600, essv5720733, essv6010334, essv5782310, essv5445780, essv6278718, essv6327570, essv5422757, essv6030157, essv5548482, essv5713465, essv5898687, essv5749868, essv5798562, essv5608095, essv6479420, essv6098926, essv5734162, essv6295527, essv5557247, essv5604658, essv5690087, essv5454848, essv5553581, essv5707095, essv5913767, essv6440448, essv5931566, essv6061041, essv5743318, essv6216131, essv5714867, essv6008598, essv5750703, essv5922039, essv6240735, essv5822170, essv5634228, essv5841751, essv6051342, essv5931765, essv6370330, essv6442483, essv5454561, essv6089033, essv6347321, essv5482046, essv5843212, essv5478805, essv6210665, essv5917158, essv6585233, essv6316149, essv5877105, essv5867778, essv5791704, essv5497707, essv6399617, essv6273385, essv6566603, essv6269396

Samples

HG00403, NA19701, HG01441, HG00442, NA19700, NA19703, HG00536, NA19397, HG00608, NA18947, HG00242, HG00524, HG01052, NA18980, NA18599, NA18999, NA20532, NA18603, HG00367, NA12340, HG00566, NA18530, HG00449, HG00150, HG00654, NA19190, HG01051, NA18633, NA18602, NA18988, HG00337, HG00663, NA19374, NA19396, HG00138, NA20796, NA19379, HG00501, NA18597, HG01351, HG01488, HG00702, HG00689, NA19723, NA18635, HG01492, HG00610, NA19062, NA18916, NA18574, NA19771, NA19088, HG01083, NA20541, HG00139, NA19720, HG00683, NA20775, NA18977, NA18868, NA19372, NA18560, NA19731, NA19075, NA18617, HG00422, HG00705, NA19087, NA18990, HG01048, NA18985, NA18908, HG00419, HG00253, NA18539, HG00108, HG01124, NA20818, NA19007, HG01353, HG00543, HG00443, NA18538, HG01171, NA19070, HG00557, HG00245, HG00428, NA19347, HG00653, HG00701, HG00657, NA20536, HG00475, NA19236, HG00583, HG00344, NA18637, HG00500, NA18948, NA18534, HG00619, HG00708, NA18548, NA18566, HG00531, HG00684, NA20538, HG01383, HG01101, HG00613, HG00525, NA19059, NA19009, NA18963, HG00704, NA18570, HG01107, NA18541, NA19012, NA19436, NA18576, NA18546, NA19401, NA19003, HG00476, NA18542, NA19834, NA18961, NA18543, NA18564, HG00565, NA19473, NA18628, NA19072, NA18950, HG00734, NA20804, NA19331, NA19835, NA19311, HG01137, NA18943, HG00256, HG00418, NA18615, HG00269, NA18501, HG00614, HG00513, NA19060, HG00656, NA19900, NA18983, HG00372, NA18984, NA18989, NA19758, NA18623, NA19065, HG00437, NA18577, HG00593

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2668847

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	163
Observed Complex	0
Frequency	n/a