A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591353



Internal ID16378762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119010267..119090661hg38UCSC Ensembl
Innerchr3:118729114..118809508hg19UCSC Ensembl
Innerchr3:120211804..120292198hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3880395
hg1980395
hg1880395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8517n54
Supporting Variantsnssv1152534
SamplesHGDP00258
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591353
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer