A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561901



Internal ID16349310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63210153..63398678hg38UCSC Ensembl
Innerchr13:63784286..63972811hg19UCSC Ensembl
Innerchr13:62682287..62870812hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38188526
hg19188526
hg18188526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812460
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561901
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