A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438276



Internal ID15041506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3825114..3830892hg38UCSC Ensembl
Innerchr18:3825114..3830892hg19UCSC Ensembl
Innerchr18:3815114..3820892hg18UCSC Ensembl
Innerchr18:3815114..3820892hg16UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385779
hg195779
hg185779
hg165779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470688, nssv470689
SamplesNA10846, NA12145
Known GenesDLGAP1
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)nsv438276
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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