Variant Details

Variant: esv2665514

Internal ID

9584933

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr19:54051962..54057368	hg38	UCSC Ensembl
Outer	chr19:54051591..54058038	hg38	UCSC Ensembl
Inner	chr19:54555216..54560622	hg19	UCSC Ensembl
Outer	chr19:54554845..54561292	hg19	UCSC Ensembl

Cytoband

19q13.42

Allele length

Assembly	Allele length
hg38	6448
hg19	6448

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv663e199

Supporting Variants

essv6009114, essv6146908, essv6043576, essv6462376, essv5941108, essv6046765, essv5565721, essv5747102, essv6406293, essv6499280, essv6553072, essv6294073, essv5626481, essv6208668, essv6262351, essv6082245, essv5406928, essv5953216, essv5882615, essv5814721, essv6043559, essv5518040, essv6367504, essv6582078, essv5879674, essv6148622, essv6238899, essv5507135, essv5476602, essv6447917, essv5998962, essv6361641, essv6187841, essv5633084, essv6077788, essv5656787, essv6434782, essv5998309, essv5796365, essv6381604, essv5530126, essv5411283, essv5632839, essv5916704, essv6563810, essv5477305, essv6195104, essv5949565, essv5459505, essv6391327

Samples

NA18502, NA19664, NA19204, NA18507, NA18486, NA19684, NA18510, NA19746, NA19171, NA18519, NA18489, NA18923, NA18916, NA19197, NA19138, NA19681, NA19720, NA19719, NA19207, NA19172, NA19722, NA19200, NA19247, NA19657, NA18934, NA19152, NA18933, NA19236, NA19654, NA19774, NA19655, NA18499, NA19750, NA19682, NA19756, NA19160, NA19652, NA19108, NA19747, NA19786, NA19783, NA19248, NA19716, NA19102, NA18873, NA19770, NA19116, NA18522, NA18487, NA19676

Known Genes

VSTM1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2665514

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	50
Observed Complex	0
Frequency	n/a