A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525746



Internal ID15453039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:23487112..23500710hg38UCSC Ensembl
Innerchr18:21067076..21080674hg19UCSC Ensembl
Innerchr18:19321074..19334672hg18UCSC Ensembl
Innerchr18:19321074..19334672hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3813599
hg1913599
hg1813599
hg1713599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701913
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525746
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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