A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901757



Internal ID15849027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54772261..54774991hg38UCSC Ensembl
Innerchr19:55283713..55286443hg19UCSC Ensembl
Innerchr19:59975525..59978255hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382731
hg192731
hg182731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580308
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)nssv901757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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