A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134678



Internal ID15987864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41521288..41629529hg38UCSC Ensembl
Innerchr9:45990557..46098798hg19UCSC Ensembl
Innerchr9:45880553..45988794hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38108242
hg19108242
hg18108242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614499
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)nssv1134678
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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