A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437864



Internal ID15041095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68041661..68043685hg38UCSC Ensembl
Innerchr3:68090811..68092835hg19UCSC Ensembl
Innerchr3:68173501..68175525hg18UCSC Ensembl
Innerchr3:68023881..68025905hg16UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382025
hg192025
hg182025
hg162025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv471282, nssv471283
SamplesNA18967, NA18940
Known GenesFAM19A1
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)nsv437864
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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