A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614081



Internal ID16401490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29981865..30040354hg38UCSC Ensembl
Innerchr9:29981863..30040352hg19UCSC Ensembl
Innerchr9:29971863..30030352hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3858490
hg1958490
hg1858490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12645n54
Supporting Variantsnssv1132485
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614081
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