A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591861



Internal ID16379270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140288452..140461721hg38UCSC Ensembl
Innerchr3:140007294..140180563hg19UCSC Ensembl
Innerchr3:141489984..141663253hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38173270
hg19173270
hg18173270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152543
Samples1780862001_A
Known GenesCLSTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591861
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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