A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv968218



Internal ID15915488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98485354..99047482hg38UCSC Ensembl
Innerchr3:98204198..98766326hg19UCSC Ensembl
Innerchr3:99686888..100249016hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38562129
hg19562129
hg18562129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591065
Supporting Variants
Samples
Known GenesCLDND1, CPOX, DCBLD2, GPR15, OR5K2, ST3GAL6, ST3GAL6-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv968218
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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