A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675578



Internal ID15065544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52307183..52394228hg38UCSC Ensembl
Innerchr12:52700967..52788012hg19UCSC Ensembl
Innerchr12:50987234..51074279hg18UCSC Ensembl
Innerchr12:50987234..51074279hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3887046
hg1987046
hg1887046
hg1787046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516938
Supporting Variants
Samples
Known GenesKRT82, KRT83, KRT84, KRT85, KRT86
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675578
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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