A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696326



Internal ID15432978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95352016..95357861hg38UCSC Ensembl
Innerchr14:95818353..95824198hg19UCSC Ensembl
Innerchr14:94888106..94893951hg18UCSC Ensembl
Innerchr14:94888106..94893951hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385846
hg195846
hg185846
hg175846
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518870
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696326
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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