A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470688



Internal ID15038129
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 StatusS
Merged Variantsnsv438276
Supporting Variants
SamplesNA12145
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)nssv470688
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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