A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv788016



Internal ID15735286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10393541..10545656hg38UCSC Ensembl
Innerchr12:10546140..10698255hg19UCSC Ensembl
Innerchr12:10437407..10589522hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38152116
hg19152116
hg18152116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557458
Supporting Variants
Samples
Known GenesKLRC1, KLRC2, KLRC3, KLRC4, KLRC4-KLRK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv788016
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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