A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722473



Internal ID19020754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35501842hg38UCSC Ensembl
Innerchr16:34470704..34736213hg19UCSC Ensembl
Innerchr16:34328205..34593714hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38265510
hg19265510
hg18265510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056564
Supporting Variants
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722473
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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