A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674631



Internal ID15411283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68605010..68607967hg38UCSC Ensembl
Innerchr14:69071727..69074684hg19UCSC Ensembl
Innerchr14:68141480..68144437hg18UCSC Ensembl
Innerchr14:68141480..68144437hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382958
hg192958
hg182958
hg172958
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516614
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674631
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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