A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv471353



Internal ID15386605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104991981..105059114hg38UCSC Ensembl
Innerchr3:104710825..104777958hg19UCSC Ensembl
Innerchr3:106193515..106260648hg18UCSC Ensembl
Innerchr3:106031726..106098859hg16UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3867134
hg1967134
hg1867134
hg1667134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437877
Supporting Variants
SamplesNA18966
Known Genes
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)nssv471353
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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