A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520546



Internal ID15101153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4157759..4164167hg38UCSC Ensembl
Innerchr18:4157759..4164167hg19UCSC Ensembl
Innerchr18:4147759..4154167hg18UCSC Ensembl
Innerchr18:4147759..4154167hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386409
hg196409
hg186409
hg176409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682597, nssv684276, nssv672417
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520546
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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