A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590123



Internal ID16377532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41489439..41546186hg38UCSC Ensembl
Innerchr3:41530930..41587677hg19UCSC Ensembl
Innerchr3:41505934..41562681hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3856748
hg1956748
hg1856748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152250
SamplesHGDP01234
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590123
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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