A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437990



Internal ID15387801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91746323..91759521hg38UCSC Ensembl
Innerchr7:91375638..91388836hg19UCSC Ensembl
Innerchr7:91213574..91226772hg18UCSC Ensembl
Innerchr7:90987667..91000865hg16UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3813199
hg1913199
hg1813199
hg1613199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv468956, nssv468957
SamplesNA18964, NA18994
Known Genes
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)nsv437990
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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