A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438151



Internal ID15041382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:110695977..110697931hg38UCSC Ensembl
InnerchrX:109939205..109941159hg19UCSC Ensembl
InnerchrX:109825861..109827815hg18UCSC Ensembl
InnerchrX:108703176..108705130hg16UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381955
hg191955
hg181955
hg161955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470212, nssv470213, nssv470214
SamplesNA19127, NA18501, NA19160
Known GenesCHRDL1
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)nsv438151
Frequency
Sample Size269
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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