A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438140



Internal ID15387951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:82140891..82156520hg38UCSC Ensembl
InnerchrX:81396340..81411969hg19UCSC Ensembl
InnerchrX:81282996..81298625hg18UCSC Ensembl
InnerchrX:80152214..80167843hg16UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3815630
hg1915630
hg1815630
hg1615630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470180, nssv470179
SamplesNA18504, NA19103
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)nsv438140
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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