A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049452



Internal ID18791983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886652..15946356hg38UCSC Ensembl
Innerchr16:15980509..16040213hg19UCSC Ensembl
Innerchr16:15888010..15947714hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3859705
hg1959705
hg1859705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2774n100
Supporting Variantsnssv3557984
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)nsv1049452
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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