A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664507



Internal ID15401159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24440534..24445351hg38UCSC Ensembl
Innerchr20:24421170..24425987hg19UCSC Ensembl
Innerchr20:24369170..24373987hg18UCSC Ensembl
Innerchr20:24369170..24373987hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384818
hg194818
hg184818
hg174818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515713
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664507
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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