A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580319



Internal ID16021042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54775343..54786119hg38UCSC Ensembl
Innerchr19:55286795..55297571hg19UCSC Ensembl
Innerchr19:59978607..59989383hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3810777
hg1910777
hg1810777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6578n54
Supporting Variantsnssv901773
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer