A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039082



Internal ID18781613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886652..15939082hg38UCSC Ensembl
Innerchr16:15980509..16032939hg19UCSC Ensembl
Innerchr16:15888010..15940440hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3852431
hg1952431
hg1852431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2774n100
Supporting Variantsnssv3557983
Samples
Known GenesFOPNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039082
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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