A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470211



Internal ID15387638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:110391989..110396827hg38UCSC Ensembl
InnerchrX:109635217..109640055hg19UCSC Ensembl
InnerchrX:109521873..109526711hg18UCSC Ensembl
InnerchrX:108399188..108404026hg16UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg384839
hg194839
hg184839
hg164839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438150
Supporting Variants
SamplesNA19211
Known GenesAMMECR1
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)nssv470211
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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