A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1133975



Internal ID15987161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38067633..38069055hg38UCSC Ensembl
Innerchr9:38067630..38069052hg19UCSC Ensembl
Innerchr9:38057630..38059052hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381423
hg191423
hg181423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614220
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)nssv1133975
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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