A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048485



Internal ID18791016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886652..15920993hg38UCSC Ensembl
Innerchr16:15980509..16014850hg19UCSC Ensembl
Innerchr16:15888010..15922351hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3834342
hg1934342
hg1834342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2773n100
Supporting Variantsnssv3557976
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)nsv1048485
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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