A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470156



Internal ID15387569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34102770..34103505hg38UCSC Ensembl
InnerchrX:34120887..34121622hg19UCSC Ensembl
InnerchrX:34030808..34031543hg18UCSC Ensembl
InnerchrX:33482313..33483048hg16UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38736
hg19736
hg18736
hg16736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438129
Supporting Variants
SamplesNA19206
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)nssv470156
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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