A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470102



Internal ID15385435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62800846..62819837hg38UCSC Ensembl
Innerchr9:66456670..66481678hg19UCSC Ensembl
Innerchr9:66196490..66221498hg18UCSC Ensembl
Innerchr9:62545375..62570383hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3818992
hg1925009
hg1825009
hg1625009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438106
Supporting Variants
SamplesNA18500
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)nssv470102
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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