A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561495



Internal ID16348904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37496412..37540973hg38UCSC Ensembl
Innerchr13:38070549..38115110hg19UCSC Ensembl
Innerchr13:36968549..37013110hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3844562
hg1944562
hg1844562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3119n54
Supporting Variantsnssv1176440
SamplesHGDP00932
Known GenesLINC00547
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561495
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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