A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591192



Internal ID16378601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103061186..103127493hg38UCSC Ensembl
Innerchr3:102780030..102846337hg19UCSC Ensembl
Innerchr3:104262720..104329027hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3866308
hg1966308
hg1866308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv970921
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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