A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438101



Internal ID15387912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33001451..33024919hg38UCSC Ensembl
Innerchr9:33001449..33024917hg19UCSC Ensembl
Innerchr9:32991449..33014917hg18UCSC Ensembl
Innerchr9:32991449..33014917hg16UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3823469
hg1923469
hg1823469
hg1623469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470095, nssv470094
SamplesNA07357, NA12057
Known GenesAPTX
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)nsv438101
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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