A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640536



Internal ID7027311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39035595..39038069hg38UCSC Ensembl
Innerchr17:39035595..39038069hg38UCSC Ensembl
Outerchr17:39035287..39038463hg38UCSC Ensembl
chr17:37191848..37194322hg19UCSC Ensembl
Innerchr17:37191848..37194322hg19UCSC Ensembl
Outerchr17:37191540..37194716hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15674227, essv15674267, essv15674216, essv15674229, essv15674273, essv15674211, essv15674285, essv15674280, essv15674209, essv15674248, essv15674264, essv15674253, essv15674287, essv15674283, essv15674239, essv15674284, essv15674257, essv15674213, essv15674224, essv15674218, essv15674270, essv15674206, essv15674237, essv15674276, essv15674291, essv15674245, essv15674261, essv15674265, essv15674281, essv15674289, essv15674231, essv15674219, essv15674260, essv15674244, essv15674233, essv15674294, essv15674274, essv15674271, essv15674254, essv15674240, essv15674212, essv15674241, essv15674256, essv15674214, essv15674268, essv15674246, essv15674222, essv15674226, essv15674293, essv15674266, essv15674255, essv15674236, essv15674230, essv15674232, essv15674225, essv15674290, essv15674269, essv15674207, essv15674238, essv15674228, essv15674215, essv15674277, essv15674295, essv15674292, essv15674251, essv15674288, essv15674279, essv15674235, essv15674221, essv15674258, essv15674286, essv15674243, essv15674205, essv15674223, essv15674282, essv15674252, essv15674242, essv15674263, essv15674208, essv15674217, essv15674234, essv15674249, essv15674220, essv15674247, essv15674272, essv15674275, essv15674250, essv15674210, essv15674262, essv15674278, essv15674259
SamplesNA20882, HG01348, HG02973, HG02648, HG02433, HG01602, NA12843, HG02337, HG02661, HG00257, HG01456, HG03667, HG01518, HG00150, HG03139, HG00097, HG03999, HG00271, NA20814, NA12812, NA18595, HG02687, NA20769, NA19649, NA07048, HG01668, HG03830, HG03817, NA20775, NA12156, HG03888, HG04238, HG00182, HG01259, HG02502, HG01198, HG01605, HG01312, HG01256, HG01524, HG03709, NA12489, HG00380, HG02793, HG03928, HG01612, HG01345, HG03781, HG00239, NA19776, HG01630, HG01092, NA20299, HG02657, HG02649, HG03643, HG04189, HG02283, HG03914, NA21143, HG03598, HG00155, HG02684, HG02696, HG02220, HG03899, HG03692, NA20351, NA19773, HG01357, HG00237, HG00662, HG02133, HG01785, HG01606, HG00111, HG02700, NA18631, NA21090, HG04014, HG03733, NA20807, HG03925, HG01781, HG00105, HG03882, HG03985, HG03931, HG03815, HG01776, HG00255
Known GenesLRRC37A11P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640536
Frequency
Sample Size2504
Observed Gain0
Observed Loss91
Observed Complex0
Frequencyn/a


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