A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515816



Internal ID15442873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52599312..52631750hg38UCSC Ensembl
Innerchr18:50125682..50158120hg19UCSC Ensembl
Innerchr18:48379680..48412118hg18UCSC Ensembl
Innerchr18:48379680..48412118hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3832439
hg1932439
hg1832439
hg1732439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664871, nssv683492
Samples
Known GenesDCC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515816
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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