A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592434



Internal ID16379843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163995763..164095964hg38UCSC Ensembl
Innerchr3:163713551..163813752hg19UCSC Ensembl
Innerchr3:165196245..165296446hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38100202
hg19100202
hg18100202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153408
SamplesNINDS_200
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592434
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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