Variant Details

Variant: esv3605854

Internal ID

6992791

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr5:96367398..96370768	hg38	UCSC Ensembl
Inner	chr5:96367398..96370768	hg38	UCSC Ensembl
Outer	chr5:96367180..96370996	hg38	UCSC Ensembl
	chr5:95703102..95706472	hg19	UCSC Ensembl
Inner	chr5:95703102..95706472	hg19	UCSC Ensembl
Outer	chr5:95702884..95706700	hg19	UCSC Ensembl

Cytoband

5q15

Allele length

Assembly	Allele length
hg38	3371
hg19	3371

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11983427, essv11983421, essv11983423, essv11983465, essv11983432, essv11983453, essv11983444, essv11983420, essv11983431, essv11983428, essv11983441, essv11983438, essv11983468, essv11983450, essv11983446, essv11983455, essv11983454, essv11983422, essv11983440, essv11983459, essv11983430, essv11983452, essv11983437, essv11983429, essv11983436, essv11983435, essv11983424, essv11983426, essv11983456, essv11983451, essv11983445, essv11983434, essv11983466, essv11983463, essv11983467, essv11983458, essv11983448, essv11983461, essv11983443, essv11983464, essv11983425, essv11983447, essv11983449, essv11983439, essv11983442, essv11983460, essv11983457, essv11983462, essv11983433

Samples

NA19466, HG03731, HG04222, HG03237, NA20878, NA21092, HG03298, HG03018, HG04164, HG03679, HG03235, HG03490, HG04070, HG03629, HG03594, HG03910, NA20896, HG01048, HG03709, HG01139, NA19347, HG03636, HG01142, NA21118, HG03781, NA20876, HG03823, NA20901, HG03824, HG01130, HG04063, HG03969, HG02725, HG01680, NA19160, HG03898, HG03774, HG03598, HG02684, HG04188, HG04134, HG01551, NA19331, NA19324, NA19360, HG04141, HG03703, NA19351, HG03815

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3605854

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	49
Observed Complex	0
Frequency	n/a