A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659113



Internal ID15395765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65296063..65304392hg38UCSC Ensembl
Innerchr14:65762781..65771110hg19UCSC Ensembl
Innerchr14:64832534..64840863hg18UCSC Ensembl
Innerchr14:64832534..64840863hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg388330
hg198330
hg188330
hg178330
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)nssv659113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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