A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696832



Internal ID15433484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75375234..75389095hg38UCSC Ensembl
Innerchr14:75841937..75855798hg19UCSC Ensembl
Innerchr14:74911690..74925551hg18UCSC Ensembl
Innerchr14:74911690..74925551hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3813862
hg1913862
hg1813862
hg1713862
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519397
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696832
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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