A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674529



Internal ID15411181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48327100..48435698hg38UCSC Ensembl
Innerchr14:48796303..48904901hg19UCSC Ensembl
Innerchr14:47866053..47974651hg18UCSC Ensembl
Innerchr14:47866053..47974651hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38108599
hg19108599
hg18108599
hg17108599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520033
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674529
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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