A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438145



Internal ID15387956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93059149..93082910hg38UCSC Ensembl
InnerchrX:92314148..92337909hg19UCSC Ensembl
InnerchrX:92200804..92224565hg18UCSC Ensembl
InnerchrX:91086005..91109766hg16UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3823762
hg1923762
hg1823762
hg1623762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470196, nssv470195
SamplesNA19159, NA19200
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)nsv438145
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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