A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580281



Internal ID16021004
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 StatusM
Merged Variants
Supporting Variantsnssv901696, nssv901697
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580281
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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