A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591863



Internal ID16032586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140407225..140555600hg38UCSC Ensembl
Innerchr3:140126067..140274442hg19UCSC Ensembl
Innerchr3:141608757..141757132hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38148376
hg19148376
hg18148376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974779
Samples
Known GenesCLSTN2, CLSTN2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591863
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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