A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1133972



Internal ID15987158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38066799..38069476hg38UCSC Ensembl
Innerchr9:38066796..38069473hg19UCSC Ensembl
Innerchr9:38056796..38059473hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg382678
hg192678
hg182678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614217
Supporting Variants
Samples
Known GenesSHB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1133972
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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