A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591266



Internal ID16031989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107385775..107957486hg38UCSC Ensembl
Innerchr3:107104622..107676333hg19UCSC Ensembl
Innerchr3:108587312..109159023hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38571712
hg19571712
hg18571712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971489
Samples
Known GenesBBX, LINC00635, LINC00636
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591266
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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