A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516109



Internal ID15443402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30223255..30282580hg38UCSC Ensembl
Innerchr18:27803220..27862545hg19UCSC Ensembl
Innerchr18:26057218..26116543hg18UCSC Ensembl
Innerchr18:26057218..26116543hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3859326
hg1959326
hg1859326
hg1759326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682110, nssv663476, nssv684148, nssv666253, nssv674277, nssv693099, nssv683837, nssv675406, nssv682842
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516109
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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