A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901641



Internal ID15848911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54716380..54815284hg38UCSC Ensembl
Innerchr19:55227879..55326739hg19UCSC Ensembl
Innerchr19:59919691..60018551hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3898905
hg1998861
hg1898861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580245
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR3DL3, LOC100287534
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901641
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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