Variant Details

Variant: esv2676664

Internal ID

9942769

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:183753151..183754483	hg38	UCSC Ensembl
Outer	chr4:183752994..183754636	hg38	UCSC Ensembl
Inner	chr4:184674304..184675636	hg19	UCSC Ensembl
Outer	chr4:184674147..184675789	hg19	UCSC Ensembl

Cytoband

4q35.1

Allele length

Assembly	Allele length
hg38	1643
hg19	1643

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5707420, essv5412998, essv5569472, essv5800956, essv6066727, essv5986540, essv5713821, essv6013848, essv5651644, essv5427554, essv5412065, essv6434064, essv6137803, essv5741265, essv6223519, essv5754137, essv6434676, essv5698737, essv5974137, essv6244726, essv6556828, essv6153243, essv6458895, essv6594367, essv5892141, essv6255278, essv5446912, essv6299190, essv5934877, essv5458296, essv6469083, essv6262898, essv6478566, essv6598411, essv5904515, essv6334855, essv6562222, essv5422809, essv6417567, essv6057335, essv5702929, essv5566359, essv5680282, essv6450704, essv6347119, essv6387125, essv6437750, essv6375798, essv5430640, essv5449125, essv6156191, essv6598446, essv6299767, essv6163599, essv5895258, essv5476750, essv5703830, essv5406416, essv6263324, essv6430101, essv6578165, essv5763578, essv5553428, essv6447064, essv5522043, essv6593594, essv5521117, essv5453642, essv6556787, essv6123794, essv6420408, essv5985959, essv6014596, essv5854841, essv6222093, essv6274411, essv6567096, essv5620848, essv6593681, essv5541242, essv6461166, essv6001802, essv6525485, essv5668895, essv6244541, essv6487871, essv5645504, essv6347064, essv5882080, essv5843292, essv6519371, essv5759712, essv5724455, essv6194813, essv5896867, essv6221767, essv5522130, essv5521321, essv5805055, essv5905548, essv5546907, essv6361262, essv6417409, essv6119447, essv5829021, essv5871324, essv5739831, essv5891331, essv6044193, essv6217661, essv6488090, essv6025985, essv6097095, essv5592031, essv6281467, essv6323389, essv5984371, essv5649110, essv6056013, essv6053691, essv5814117, essv6501729, essv6513996, essv5780186, essv5837932, essv5665522, essv5686327, essv5699915, essv6210339, essv6237028, essv6384674, essv5692936, essv6537050, essv5939082, essv6478985, essv5760697, essv5678260, essv5583684, essv5959760, essv6276790, essv5420799, essv6528323, essv5536564

Samples

HG00403, HG00542, HG00442, HG01173, HG01356, HG00608, HG00142, HG00671, NA19066, HG00242, NA18592, HG01359, HG00187, HG01188, HG00315, HG00306, NA12340, NA18616, HG00654, NA19443, HG00261, NA12750, NA18602, NA18988, NA12341, HG00327, NA19107, HG00641, NA19381, NA19076, HG01366, NA18595, NA18982, NA12348, HG01492, HG00334, HG00185, HG00311, HG00243, NA19079, HG00281, NA20759, HG01069, HG01080, NA19383, HG00683, HG00335, HG00148, HG00106, HG01170, HG00325, HG00232, NA19471, HG00705, NA19722, NA19901, HG00118, NA19189, HG00159, NA18557, NA18985, HG00326, HG00323, HG00253, HG00108, NA11831, HG00543, HG00188, NA19082, HG01187, NA19070, NA19056, HG00557, NA19077, HG00732, HG00475, HG00436, HG00584, HG00583, NA19081, NA18534, NA19654, HG00324, HG01073, HG00273, HG00651, NA19084, HG01197, HG00331, NA20538, HG01101, HG00525, HG00140, NA19059, HG01334, NA19009, HG00152, NA18963, HG00126, NA18593, HG01204, NA18576, NA19685, HG00258, HG00476, NA19440, HG00119, HG01190, HG00336, HG00285, HG00366, HG00136, HG00638, HG00278, HG01174, HG00473, HG00256, NA19085, NA18615, NA18610, HG00125, NA19078, HG00478, NA19248, HG01055, HG00698, NA18552, NA19900, NA19661, HG01377, NA18984, NA19430, NA19004, HG01125, HG00171, NA12890, NA18623, NA18612, HG01191, NA20754, HG00553, NA18620, 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)

esv2676664

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	143
Observed Complex	0
Frequency	n/a