A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958028



Internal ID15905298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4084575..4283616hg38UCSC Ensembl
Innerchr3:4126259..4325300hg19UCSC Ensembl
Innerchr3:4101259..4300300hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38199042
hg19199042
hg18199042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589428
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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