A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589242



Internal ID16029965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47730..388999hg38UCSC Ensembl
Innerchr3:89412..430682hg19UCSC Ensembl
Innerchr3:64412..405682hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38341270
hg19341271
hg18341271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957555
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589242
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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