A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901698



Internal ID15848968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54764062..54776705hg38UCSC Ensembl
Innerchr19:55275514..55288157hg19UCSC Ensembl
Innerchr19:59967326..59979969hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3812644
hg1912644
hg1812644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580282
Supporting Variants
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901698
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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