A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697886



Internal ID15434538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69651450..69655485hg38UCSC Ensembl
Innerchr10:71411206..71415241hg19UCSC Ensembl
Innerchr10:71081212..71085247hg18UCSC Ensembl
Innerchr10:71081212..71085247hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384036
hg194036
hg184036
hg174036
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521284
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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