A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526858



Internal ID15454151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14940294..14954304hg38UCSC Ensembl
Innerchr18:14940293..14954303hg19UCSC Ensembl
Innerchr18:14930293..14944303hg18UCSC Ensembl
Innerchr18:14930293..14944303hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3814011
hg1914011
hg1814011
hg1714011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703216
Samples
Known GenesLOC400644
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526858
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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