A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613883



Internal ID16401292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24645078..24731625hg38UCSC Ensembl
Innerchr9:24645076..24731623hg19UCSC Ensembl
Innerchr9:24635076..24721623hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3886548
hg1986548
hg1886548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12609n54
Supporting Variantsnssv1132013
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613883
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