A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528616



Internal ID15109223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52756581..52768744hg38UCSC Ensembl
Innerchr12:53150365..53162528hg19UCSC Ensembl
Innerchr12:51436632..51448795hg18UCSC Ensembl
Innerchr12:51436632..51448795hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3812164
hg1912164
hg1812164
hg1712164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705245
Samples
Known GenesKRT76
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528616
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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