A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901653



Internal ID15848923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54748501..54773045hg38UCSC Ensembl
Innerchr19:55259953..55284497hg19UCSC Ensembl
Innerchr19:59951765..59976309hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824545
hg1924545
hg1824545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580256
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901653
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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