A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591269



Internal ID16378678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109728616..109777182hg38UCSC Ensembl
Innerchr3:109447463..109496029hg19UCSC Ensembl
Innerchr3:110930153..110978719hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3848567
hg1948567
hg1848567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152522
SamplesHGDP00881
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591269
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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