A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958043



Internal ID15905313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4151816..4225160hg38UCSC Ensembl
Innerchr3:4193500..4266844hg19UCSC Ensembl
Innerchr3:4168500..4241844hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3873345
hg1973345
hg1873345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589444
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)nssv958043
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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