A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661252



Internal ID15397904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65279848..65297839hg38UCSC Ensembl
Innerchr14:65746566..65764557hg19UCSC Ensembl
Innerchr14:64816319..64834310hg18UCSC Ensembl
Innerchr14:64816319..64834310hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3817992
hg1917992
hg1817992
hg1717992
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515522
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661252
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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