A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559982



Internal ID18511577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88025957..88349961hg38UCSC Ensembl
Innerchr16:88059563..88383567hg19UCSC Ensembl
Innerchr16:86617064..86941068hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38324005
hg19324005
hg18324005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058465
Supporting Variants
Samples
Known GenesBANP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559982
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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