A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589294



Internal ID16030017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:396570..677870hg38UCSC Ensembl
Innerchr3:438253..719554hg19UCSC Ensembl
Innerchr3:413253..694554hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38281301
hg19281302
hg18281302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957805
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589294
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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