A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437949



Internal ID15041180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168768097..168772928hg38UCSC Ensembl
Innerchr4:169689248..169694079hg19UCSC Ensembl
Innerchr4:169925823..169930654hg18UCSC Ensembl
Innerchr4:170385138..170389969hg16UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg384832
hg194832
hg184832
hg164832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv468667, nssv468666
SamplesNA18861, NA18852
Known GenesPALLD
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)nsv437949
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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