A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634102



Internal ID7020906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37889605..37896606hg38UCSC Ensembl
Innerchr14:37889829..37896554hg38UCSC Ensembl
Outerchr14:37889460..37896751hg38UCSC Ensembl
chr14:38358810..38365811hg19UCSC Ensembl
Innerchr14:38359034..38365759hg19UCSC Ensembl
Outerchr14:38358665..38365956hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg387002
hg197002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14970202, essv14970209, essv14970203, essv14970213, essv14970196, essv14970212, essv14970214, essv14970200, essv14970197, essv14970205, essv14970201, essv14970195, essv14970204, essv14970207, essv14970211, essv14970199, essv14970198, essv14970215, essv14970210, essv14970208, essv14970206
SamplesNA20774, HG01083, HG03762, NA20764, HG01942, HG02697, HG01612, HG01619, NA20538, NA06989, HG00117, HG00126, NA20815, HG03727, HG01342, NA20897, HG01105, HG03882, NA20585, HG00362, NA12776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634102
Frequency
Sample Size2504
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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