A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549125



Internal ID18500720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23388873..23497409hg38UCSC Ensembl
Innerchr16:23400194..23508730hg19UCSC Ensembl
Innerchr16:23307695..23416231hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38108537
hg19108537
hg18108537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066078
Supporting Variants
Samples
Known GenesCOG7, GGA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3549125
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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