A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591351



Internal ID16378760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119010267..119070756hg38UCSC Ensembl
Innerchr3:118729114..118789603hg19UCSC Ensembl
Innerchr3:120211804..120272293hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3860490
hg1960490
hg1860490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8516n54
Supporting Variantsnssv971641
Samples
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591351
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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