A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521537



Internal ID15448830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67520929..67636040hg38UCSC Ensembl
Innerchr18:65188166..65303277hg19UCSC Ensembl
Innerchr18:63339146..63454257hg18UCSC Ensembl
Innerchr18:63339146..63454257hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38115112
hg19115112
hg18115112
hg17115112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698153
Samples
Known GenesLOC643542
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521537
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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