A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv471291



Internal ID15386886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89353712..89367914hg38UCSC Ensembl
Innerchr3:89402862..89417064hg19UCSC Ensembl
Innerchr3:89485552..89499754hg18UCSC Ensembl
Innerchr3:89323763..89337965hg16UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3814203
hg1914203
hg1814203
hg1614203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437866
Supporting Variants
SamplesNA19007
Known GenesEPHA3
MethodSNP array
AnalysisNull genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nssv471291
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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