A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695903



Internal ID15432555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22550221..22562933hg38UCSC Ensembl
Innerchr14:23019164..23031833hg19UCSC Ensembl
Innerchr14:22089004..22101673hg18UCSC Ensembl
Innerchr14:22089004..22101673hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3812713
hg1912670
hg1812670
hg1712670
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518467
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695903
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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