A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1131396



Internal ID15984582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22606576..22619734hg38UCSC Ensembl
Innerchr9:22606575..22619733hg19UCSC Ensembl
Innerchr9:22596575..22609733hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3813159
hg1913159
hg1813159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613785
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1131396
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