A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698885



Internal ID15435537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14584727..14734476hg38UCSC Ensembl
Innerchr18:14584726..14734475hg19UCSC Ensembl
Innerchr18:14574726..14724475hg18UCSC Ensembl
Innerchr18:14574726..14724475hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38149750
hg19149750
hg18149750
hg17149750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523173
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698885
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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