A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559979



Internal ID18511574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87104663..87368138hg38UCSC Ensembl
Innerchr16:87138269..87401744hg19UCSC Ensembl
Innerchr16:85695770..85959245hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38263476
hg19263476
hg18263476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062525
Supporting Variants
Samples
Known GenesC16orf95, FBXO31, LOC101928682
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559979
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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