A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502884



Internal ID18454479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10344125..10444121hg38UCSC Ensembl
Innerchr12:10496724..10596720hg19UCSC Ensembl
Innerchr12:10387991..10487987hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3899997
hg1999997
hg1899997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036390
Supporting Variants
Samples
Known GenesKLRC2, KLRC3, KLRC4, KLRC4-KLRK1, KLRK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502884
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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