A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438147



Internal ID15387958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97716126..97730402hg38UCSC Ensembl
InnerchrX:96971125..96985401hg19UCSC Ensembl
InnerchrX:96857781..96872057hg18UCSC Ensembl
InnerchrX:95742982..95757258hg16UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3814277
hg1914277
hg1814277
hg1614277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470203
SamplesNA18611
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)nsv438147
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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