A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152459



Internal ID15506961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4103854..4140066hg38UCSC Ensembl
Innerchr3:4145538..4181750hg19UCSC Ensembl
Innerchr3:4120538..4156750hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3836213
hg1936213
hg1836213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589437
Supporting Variants
Samples1780854328_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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