A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437942



Internal ID15041173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150959613..150962566hg38UCSC Ensembl
Innerchr4:151880765..151883718hg19UCSC Ensembl
Innerchr4:152100215..152103168hg18UCSC Ensembl
Innerchr4:152458392..152461345hg16UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382954
hg192954
hg182954
hg162954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv468637, nssv468636, nssv468638, nssv468639
SamplesNA19210, NA19143, NA19211, NA19239
Known GenesLRBA
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)nsv437942
Frequency
Sample Size269
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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