A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718838



Internal ID18670433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5466061..5752374hg38UCSC Ensembl
Innerchr16:5516062..5802375hg19UCSC Ensembl
Innerchr16:5456063..5742376hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38286314
hg19286314
hg18286314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048972
Supporting Variants
Samples
Known GenesMIR8065
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718838
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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