Variant Details

Variant: esv2672538

Internal ID

9938643

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:68691227..68691883	hg38	UCSC Ensembl
Outer	chr15:68690856..68692253	hg38	UCSC Ensembl
Inner	chr15:68983566..68984222	hg19	UCSC Ensembl
Outer	chr15:68983195..68984592	hg19	UCSC Ensembl

Cytoband

15q23

Allele length

Assembly	Allele length
hg38	1398
hg19	1398

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5760758, essv6455371, essv6185339, essv5418068, essv6441884, essv6387185, essv5521363, essv5455392, essv6043875, essv5917807, essv6480527, essv5785908, essv5577569, essv5884623, essv6590665, essv5476628, essv6000449, essv6057457, essv5397060, essv5574977, essv6331282, essv5979937, essv6207512, essv6417178, essv5875260, essv5794728, essv5777206, essv5841077, essv6111121, essv6536542, essv6295084, essv6427065, essv6256711, essv6310191, essv6328835, essv5404731, essv5837435, essv5671401, essv6391627, essv6423147, essv5760378, essv5657124, essv6375877, essv5878830, essv5796890, essv5682770, essv5632331, essv6089616, essv5946010, essv6495686, essv5670640, essv6500001, essv6519165, essv6346759, essv6114292, essv6284551, essv6513161, essv6430801, essv5712194, essv6063969, essv6420062, essv6012897, essv5610771, essv5541120, essv5742961, essv6433756, essv6249491, essv6079369, essv5693995, essv5591333, essv6128862, essv6542755, essv6596121, essv5495658, essv6056584, essv6278404, essv6137763, essv5629314, essv6285473, essv5521467, essv6358833, essv6086535, essv6010163, essv6395133, essv6021804, essv5732355, essv6519297

Samples

HG00593, HG00626, HG00403, HG00650, HG00542, HG00442, HG00536, HG00608, HG00671, HG00559, HG00524, HG00699, HG00566, HG00449, HG00654, HG00693, HG00589, HG00501, HG00702, HG00689, HG00448, HG00634, HG00610, HG00537, HG00590, HG00512, HG00683, HG00534, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00629, HG00443, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00635, 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

CORO2B

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2672538

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	87
Observed Complex	0
Frequency	n/a