A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438132



Internal ID15387943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56925030..56929603hg38UCSC Ensembl
InnerchrX:56951463..56956036hg19UCSC Ensembl
InnerchrX:56968188..56972761hg18UCSC Ensembl
InnerchrX:55918254..55922827hg16UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg384574
hg194574
hg184574
hg164574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470164, nssv470165
SamplesNA18504, NA19138
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)nsv438132
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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