A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699906



Internal ID15436558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98598992..98717344hg38UCSC Ensembl
Innerchr3:98317836..98436188hg19UCSC Ensembl
Innerchr3:99800526..99918878hg18UCSC Ensembl
Innerchr3:99800526..99918878hg17UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38118353
hg19118353
hg18118353
hg17118353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524042
Supporting Variants
Samples
Known GenesST3GAL6-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699906
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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