A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665920



Internal ID9932025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102171229..102173355hg38UCSC Ensembl
Outerchr14:102171172..102173410hg38UCSC Ensembl
Innerchr14:102637566..102639692hg19UCSC Ensembl
Outerchr14:102637509..102639747hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5910054, essv6585847, essv6462693, essv5644812, essv6142080, essv6089052, essv5521565, essv6117250, essv6021575, essv6168233, essv6166115, essv6137247, essv6559554, essv6438867, essv5460872
SamplesNA20761, NA12045, HG00179, NA19678, NA20795, HG00247, HG00156, HG01176, NA19722, HG00239, HG00258, HG00278, HG00112, NA20826, HG00274
Known GenesWDR20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665920
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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