A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591962



Internal ID16379371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146794966..146851250hg38UCSC Ensembl
Innerchr3:146512753..146569037hg19UCSC Ensembl
Innerchr3:147995443..148051727hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3856285
hg1956285
hg1856285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152275
SamplesHGDP00963
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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