A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152533



Internal ID15881313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119010267..119083007hg38UCSC Ensembl
Innerchr3:118729114..118801854hg19UCSC Ensembl
Innerchr3:120211804..120284544hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3872741
hg1972741
hg1872741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591352
Supporting Variants
SamplesNINDS_99
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152533
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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