A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695216



Internal ID15431868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68569053..68660077hg38UCSC Ensembl
Innerchr18:66236290..66327314hg19UCSC Ensembl
Innerchr18:64387270..64478294hg18UCSC Ensembl
Innerchr18:64387270..64478294hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3891025
hg1991025
hg1891025
hg1791025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517811
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695216
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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