A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132505



Internal ID15639005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30420640..30698144hg38UCSC Ensembl
Innerchr9:30420638..30698142hg19UCSC Ensembl
Innerchr9:30410638..30688142hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38277505
hg19277505
hg18277505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614097
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)nssv1132505
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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