A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438141



Internal ID15041372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85932135..85945124hg38UCSC Ensembl
InnerchrX:85187140..85200129hg19UCSC Ensembl
InnerchrX:85073796..85086785hg18UCSC Ensembl
InnerchrX:83958997..83971986hg16UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3812990
hg1912990
hg1812990
hg1612990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470181, nssv470182
SamplesNA18540, NA18532
Known GenesCHM
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)nsv438141
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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