A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524650



Internal ID15451943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67544901..67654665hg38UCSC Ensembl
Innerchr18:65212138..65321902hg19UCSC Ensembl
Innerchr18:63363118..63472882hg18UCSC Ensembl
Innerchr18:63363118..63472882hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38109765
hg19109765
hg18109765
hg17109765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700616
Samples
Known GenesLOC643542
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524650
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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