A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591267



Internal ID16378676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107963250..107995228hg38UCSC Ensembl
Innerchr3:107682097..107714075hg19UCSC Ensembl
Innerchr3:109164787..109196765hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3831979
hg1931979
hg1831979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971490
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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