Variant Details

Variant: esv3598695

Internal ID

6985830

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:173507638..173601328	hg38	UCSC Ensembl
	chr3:173225428..173319118	hg19	UCSC Ensembl

Cytoband

3q26.31

Allele length

Assembly	Allele length
hg38	93691
hg19	93691

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11228798, essv11228797, essv11228761, essv11228774, essv11228753, essv11228773, essv11228769, essv11228782, essv11228790, essv11228795, essv11228763, essv11228750, essv11228766, essv11228751, essv11228777, essv11228799, essv11228749, essv11228758, essv11228784, essv11228762, essv11228785, essv11228778, essv11228756, essv11228767, essv11228791, essv11228765, essv11228800, essv11228768, essv11228771, essv11228755, essv11228787, essv11228770, essv11228788, essv11228776, essv11228757, essv11228775, essv11228759, essv11228801, essv11228794, essv11228796, essv11228793, essv11228764, essv11228779, essv11228780, essv11228786, essv11228754, essv11228781, essv11228760, essv11228792, essv11228752, essv11228772, essv11228783, essv11228789

Samples

NA20543, HG01961, NA20332, NA12155, HG01506, HG00109, HG01702, NA19762, HG01968, NA20905, NA19782, NA19681, HG02278, HG04214, HG02736, HG01950, NA20845, HG00743, HG00133, HG02265, HG01248, HG01171, HG02236, HG04195, HG01979, NA20314, NA20862, HG01989, HG04180, HG04155, NA19740, HG02292, HG03991, HG01992, NA21113, NA12716, HG01954, HG02223, NA20276, NA20804, NA20778, NA19741, HG04141, HG00125, NA19759, HG00111, NA21090, NA19780, HG01468, HG02681, HG01920, NA11892, HG01111

Known Genes

NLGN1

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3598695

Frequency

Sample Size	2504
Observed Gain	53
Observed Loss	0
Observed Complex	0
Frequency	n/a