A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591272



Internal ID16378681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110288358..110436977hg38UCSC Ensembl
Innerchr3:110007205..110155824hg19UCSC Ensembl
Innerchr3:111489895..111638514hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38148620
hg19148620
hg18148620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152523
SamplesHGDP00529
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591272
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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