A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438162



Internal ID15041393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155545002..155547903hg38UCSC Ensembl
InnerchrX:154774663..154777564hg19UCSC Ensembl
InnerchrX:154427857..154430758hg18UCSC Ensembl
InnerchrX:153206494..153209395hg16UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382902
hg192902
hg182902
hg162902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470236
SamplesNA12003
Known GenesTMLHE
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)nsv438162
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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