A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470204



Internal ID15040979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:109655135..109668538hg38UCSC Ensembl
InnerchrX:108898364..108911767hg19UCSC Ensembl
InnerchrX:108785020..108798423hg18UCSC Ensembl
InnerchrX:107662335..107675738hg16UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3813404
hg1913404
hg1813404
hg1613404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438149
Supporting Variants
SamplesNA19223
Known GenesACSL4
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)nssv470204
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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