A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv468929



Internal ID15384532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90181213..90182815hg38UCSC Ensembl
Innerchr7:89810527..89812129hg19UCSC Ensembl
Innerchr7:89648463..89650065hg18UCSC Ensembl
Innerchr7:89422556..89424158hg16UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381603
hg191603
hg181603
hg161603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437989
Supporting Variants
SamplesNA11830
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)nssv468929
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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