A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438121



Internal ID15387932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7431479..7599284hg38UCSC Ensembl
InnerchrX:7349520..7517325hg19UCSC Ensembl
InnerchrX:7359520..7527325hg18UCSC Ensembl
InnerchrX:6811025..6978830hg16UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38167806
hg19167806
hg18167806
hg16167806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470134, nssv470135, nssv470136
SamplesNA12248, NA10854
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)nsv438121
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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