A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667828



Internal ID15404480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120961092..121076655hg38UCSC Ensembl
Innerchr5:120296787..120412350hg19UCSC Ensembl
Innerchr5:120324686..120440249hg18UCSC Ensembl
Innerchr5:120324686..120440249hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38115564
hg19115564
hg18115564
hg17115564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517000
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667828
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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