A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661271



Internal ID15397923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73250066..73271334hg38UCSC Ensembl
Innerchr14:73716774..73738042hg19UCSC Ensembl
Innerchr14:72786527..72807795hg18UCSC Ensembl
Innerchr14:72786527..72807795hg17UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3821269
hg1921269
hg1821269
hg1721269
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516851
Supporting Variants
Samples
Known GenesPAPLN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661271
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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