A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1133969



Internal ID15987155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36487307..36488264hg38UCSC Ensembl
Innerchr9:36487304..36488261hg19UCSC Ensembl
Innerchr9:36477304..36478261hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38958
hg19958
hg18958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614210
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)nssv1133969
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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