A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737484



Internal ID19035765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:46675963..46750478hg38UCSC Ensembl
Innerchr22:47071860..47146375hg19UCSC Ensembl
Innerchr22:45450524..45525039hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3874516
hg1974516
hg1874516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060721
Supporting Variants
Samples
Known GenesCERK, GRAMD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3737484
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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