A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438269



Internal ID15041499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34429609..34516780hg38UCSC Ensembl
Innerchr15:34721810..34808981hg19UCSC Ensembl
Innerchr15:32509102..32596273hg18UCSC Ensembl
Innerchr15:32437866..32525037hg16UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3887172
hg1987172
hg1887172
hg1687172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470661, nssv470664, nssv470662
SamplesNA18500, NA18521, NA19144
Known GenesGOLGA8A
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)nsv438269
Frequency
Sample Size269
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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