A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152455



Internal ID15526953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4093768..4124049hg38UCSC Ensembl
Innerchr3:4135452..4165733hg19UCSC Ensembl
Innerchr3:4110452..4140733hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3830282
hg1930282
hg1830282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589430
Supporting Variants
SamplesHGDP00279
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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