A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700476



Internal ID15090442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21820676..21919143hg38UCSC Ensembl
Innerchr14:22288841..22387318hg19UCSC Ensembl
Innerchr14:21358681..21457158hg18UCSC Ensembl
Innerchr14:21358681..21457158hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3898468
hg1998478
hg1898478
hg1798478
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524527
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700476
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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