A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592673



Internal ID16380082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184751325..184754681hg38UCSC Ensembl
Innerchr3:184469113..184472469hg19UCSC Ensembl
Innerchr3:185951807..185955163hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg383357
hg193357
hg183357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8759n54
Supporting Variantsnssv982577
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592673
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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