A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901696



Internal ID15848966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54761683..54773045hg38UCSC Ensembl
Innerchr19:55273135..55284497hg19UCSC Ensembl
Innerchr19:59964947..59976309hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811363
hg1911363
hg1811363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580281
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)nssv901696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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