Variant Details

Variant: esv2658348

Internal ID

9577767

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:74963788..75064509	hg38	UCSC Ensembl
Outer	chr7:74963417..75064879	hg38	UCSC Ensembl
Inner	chr7:74378516..74480322	hg19	UCSC Ensembl
Outer	chr7:74378145..74480692	hg19	UCSC Ensembl

Cytoband

7q11.23

Allele length

Assembly	Allele length
hg38	101463
hg19	102548

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5622934, essv6021596, essv6175304, essv5461832, essv5678732, essv5924722, essv6396768, essv6125037, essv6259828, essv6242704, essv5570353, essv5986219, essv5792780, essv6535866, essv5843065, essv6153701, essv5578433, essv6088156, essv6072479, essv6214769, essv6257456, essv6522041, essv5532927, essv5975609, essv6413994, essv5548265, essv5647098, essv6299414, essv5973375, essv6491313, essv6353839, essv6475624, essv5452737, essv6104132, essv6033560, essv5801001, essv6341446, essv6548183, essv5976076, essv6325464, essv6277342, essv6399805, essv5646734, essv5884828, essv5837623, essv5508410, essv6570831, essv5502631, essv5751239, essv5831587, essv5740038, essv5478732, essv6136923, essv6436958, essv5649460, essv5862206, essv5760084, essv6501232, essv6547555, essv6021554, essv5944455, essv6285501, essv5485171, essv6520990, essv6047220, essv6409112, essv6318703, essv6559800, essv5676110, essv6343784, essv5631842, essv6506647, essv5972393, essv5734143, essv5890553, essv5950934, essv5590147, essv5872050, essv5518608, essv6394118, essv6359166, essv6532953, essv6064582, essv5993526, essv6079162, essv5834203, essv6435222, essv5918765, essv6111891, essv5904276, essv6458865, essv5623062

Samples

HG00593, HG00626, HG00403, HG00650, HG00542, HG00442, HG00592, HG00536, HG00608, HG00671, HG00559, HG00524, HG00699, HG00566, HG00449, HG00654, HG00693, HG00663, HG00589, HG00501, HG00702, HG00689, HG00448, HG00634, HG00610, HG00537, HG00590, HG00512, HG00683, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00560, HG00629, HG00443, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00635, HG00651, HG00690, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00625, HG00565, HG00580, HG00473, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00595, HG00472, HG00628, HG00437, HG00581

Known Genes

WBSCR16

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2658348

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	92
Observed Complex	0
Frequency	n/a