A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132050



Internal ID15985236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25638011..25667664hg38UCSC Ensembl
Innerchr9:25638009..25667662hg19UCSC Ensembl
Innerchr9:25628009..25657662hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3829654
hg1929654
hg1829654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613918
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)nssv1132050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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