A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv795993



Internal ID15743263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52313066..52315194hg38UCSC Ensembl
Innerchr12:52706850..52708978hg19UCSC Ensembl
Innerchr12:50993117..50995245hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg382129
hg192129
hg182129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558923
Supporting Variants
Samples
Known GenesKRT83
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv795993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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