Variant Details

Variant: esv2656946

Internal ID

9576365

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr16:17381891..17385889	hg38	UCSC Ensembl
	chr16:17475748..17479746	hg19	UCSC Ensembl

Cytoband

16p12.3

Allele length

Assembly	Allele length
hg38	3999
hg19	3999

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv482e199

Supporting Variants

essv6368239, essv6175489, essv6221982, essv5503437, essv6500844, essv5874890, essv5625648, essv5489256, essv6492460, essv6066170, essv6549576, essv6010554, essv6446341, essv5735313, essv5912368, essv6279707, essv6175009, essv6035587, essv6517925, essv5949871, essv6348366, essv6299616, essv5430937, essv5532733, essv5910077, essv5509738, essv5728740, essv5948591, essv5503724, essv5467004, essv6083404, essv5920101, essv6172769, essv5689919, essv5977234, essv6208173, essv6591009, essv6231917, essv5844509, essv6253967, essv6122929, essv5765511, essv6344163, essv6121470, essv5996341, essv6015040, essv5772990, essv6281879, essv5781207, essv6059519, essv6230365, essv6178838, essv5625784, essv5582432, essv6175453, essv6067680, essv5696027

Samples

HG00403, NA19058, HG00671, NA19066, HG01066, NA18633, HG00663, HG01070, NA19651, NA18617, NA19725, HG01198, HG00464, HG00560, NA18613, HG00629, NA19070, NA19056, NA12878, HG00701, HG00436, HG00556, NA19081, NA19788, NA18534, HG00619, NA19064, NA18537, HG00404, HG00531, HG01197, HG00613, HG00525, NA19009, NA18963, NA19225, NA18634, HG01107, NA18541, NA19012, NA19652, NA18535, NA18941, HG00473, NA19085, HG00707, HG00614, NA19779, HG00421, NA18987, NA19213, NA18989, NA18623, NA19074, HG00437, NA18965, NA18620

Known Genes

XYLT1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2656946

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	57
Observed Complex	0
Frequency	n/a