A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470134



Internal ID15384352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7465307..7570484hg38UCSC Ensembl
InnerchrX:7383348..7488525hg19UCSC Ensembl
InnerchrX:7393348..7498525hg18UCSC Ensembl
InnerchrX:6844853..6950030hg16UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38105178
hg19105178
hg18105178
hg16105178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438121
Supporting Variants
SamplesNA10854
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)nssv470134
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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