A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958029



Internal ID15905299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4087093..4120059hg38UCSC Ensembl
Innerchr3:4128777..4161743hg19UCSC Ensembl
Innerchr3:4103777..4136743hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3832967
hg1932967
hg1832967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589429
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)nssv958029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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