Variant Details

Variant: esv2666932

Internal ID

9933037

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:82371170..82482204	hg38	UCSC Ensembl
Outer	chr15:82370798..82482570	hg38	UCSC Ensembl
Inner	chr15:83039916..83150922	hg19	UCSC Ensembl
Outer	chr15:83039545..83151292	hg19	UCSC Ensembl

Cytoband

15q25.2

Allele length

Assembly	Allele length
hg38	111773
hg19	111748

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6465436, essv5790887, essv6390999, essv5707125, essv6430536, essv5883449, essv5808595, essv5980874, essv6458329, essv6100411, essv6117792, essv5906120, essv6453791, essv6535803, essv6339582, essv6477863, essv5952923, essv5640459, essv5845211, essv5869612, essv6055396, essv6286063, essv5839007, essv6449569, essv6303040, essv6232112, essv6456827, essv5945838, essv5450843, essv6074241, essv5798658, essv5866733, essv5513380, essv5843639, essv5533006, essv5906434, essv6579680, essv5677938, essv6512183, essv6499709, essv6072414, essv6359989, essv6446826, essv6328388, essv5992572, essv5586164, essv5559110, essv5903657, essv6286797, essv6052882, essv6454736, essv6071802, essv6553175, essv6508967, essv6013527, essv5943610, essv6439690, essv6291322, essv5647426, essv5479657, essv5774994, essv6072809, essv5776172, essv5883574, essv5532125, essv5509812, essv6537381, essv6478904, essv6102463, essv5595362, essv5930860, essv6502064, essv5916500, essv6112571, essv5726690, essv5979043, essv6487511, essv5918557, essv6051990, essv6012700, essv5710068, essv5691276, essv5866518, essv6324345, essv6395603, essv6348810, essv6130643, essv5432991, essv6079809, essv5633911

Samples

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, 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

CSPG4P8, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, UBE2Q2P2, UBE2Q2P3

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2666932

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	90
Observed Complex	0
Frequency	n/a