A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666176



Internal ID9932281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:874621..874730hg38UCSC Ensembl
Outerchr17:874584..874780hg38UCSC Ensembl
Innerchr17:777861..777970hg19UCSC Ensembl
Outerchr17:777824..778020hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5801511, essv5580967, essv5580868, essv6341551, essv6027885, essv5493861, essv5720367, essv5671390, essv6510202, essv6040639, essv5807837, essv6130482, essv6108083, essv5761359, essv6227659, essv5996348, essv6214548, essv6543371, essv5756232, essv6143813, essv6243818, essv6479321
SamplesNA19394, HG00315, HG01070, HG01488, HG00330, HG01492, NA19404, NA19371, HG00326, HG00282, HG00275, NA18566, HG01073, HG00651, HG00531, HG00525, HG00237, HG00319, NA19360, NA18610, HG00259, HG01082
Known GenesNXN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666176
Frequency
Sample Size1151
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer