Variant Details

Variant: esv2665410

Internal ID

9931515

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:57294906..57295500	hg38	UCSC Ensembl
	chr15:57587104..57587698	hg19	UCSC Ensembl

Cytoband

15q21.3

Allele length

Assembly	Allele length
hg38	595
hg19	595

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5600222, essv5573182, essv6198551, essv6354388, essv6295680, essv5434279, essv5968850, essv5816485, essv6030945, essv5498527, essv6465187, essv6220728, essv6017031, essv6087615, essv5621754, essv5512684, essv6514816, essv6595144, essv6468390, essv6497333, essv6092290, essv6074820, essv5622648, essv5641756, essv5560737, essv5960788, essv5670532, essv6511711, essv5408718, essv6349363, essv6269258, essv5490828, essv6461410, essv5837472, essv6449819, essv6422748, essv6339428, essv5668339, essv6119676, essv5438291, essv6129132, essv5726877, essv6097100, essv5694108, essv5457804, essv6520517, essv6587696, essv5790799, essv5818027, essv5928192, essv6463576, essv6593657, essv5933912, essv5878751, essv6590351, essv5587712

Samples

HG01441, HG01173, NA19664, HG00242, HG01052, NA12414, NA11931, HG00244, HG01051, HG00337, NA19660, HG01366, HG01492, HG00346, HG00369, HG01365, HG00158, HG00139, HG00277, HG01069, NA19720, NA19651, HG01080, HG01067, HG00148, NA12156, HG01170, HG00262, HG00232, HG01176, HG01440, NA19722, HG01136, HG00731, NA19717, NA19663, NA19788, HG01149, HG01073, HG00321, HG01497, HG00276, HG01107, NA19675, NA19685, HG00734, NA07051, HG01375, NA19679, NA20803, NA19783, HG00339, NA19726, HG01377, NA18511, HG01191

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2665410

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	56
Observed Complex	0
Frequency	n/a