A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132512



Internal ID15639012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30520324..30733388hg38UCSC Ensembl
Innerchr9:30520322..30733386hg19UCSC Ensembl
Innerchr9:30510322..30723386hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38213065
hg19213065
hg18213065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614104
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)nssv1132512
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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