A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613401



Internal ID16400810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10661677..10688795hg38UCSC Ensembl
Innerchr9:10661677..10688795hg19UCSC Ensembl
Innerchr9:10651677..10678795hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3827119
hg1927119
hg1827119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12520n54
Supporting Variantsnssv1128526
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613401
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