A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520945



Internal ID15448238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14076973..14265835hg38UCSC Ensembl
Innerchr18:14076972..14265834hg19UCSC Ensembl
Innerchr18:14066972..14255834hg18UCSC Ensembl
Innerchr18:14066972..14255834hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38188863
hg19188863
hg18188863
hg17188863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697702
Samples
Known GenesANKRD20A5P, ZNF519
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520945
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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