A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591356



Internal ID16378765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119012458..119090661hg38UCSC Ensembl
Innerchr3:118731305..118809508hg19UCSC Ensembl
Innerchr3:120213995..120292198hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3878204
hg1978204
hg1878204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8517n54
Supporting Variantsnssv1152535
SamplesHGDP00058
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591356
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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