A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv788014



Internal ID15735284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10379727..10545656hg38UCSC Ensembl
Innerchr12:10532326..10698255hg19UCSC Ensembl
Innerchr12:10423593..10589522hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38165930
hg19165930
hg18165930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557456
Supporting Variants
Samples
Known GenesKLRC1, KLRC2, KLRC3, KLRC4, KLRC4-KLRK1, KLRK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv788014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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