A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063064



Internal ID18805595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85070279..85219999hg38UCSC Ensembl
Innerchr16:85103885..85253605hg19UCSC Ensembl
Innerchr16:83661386..83811106hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38149721
hg19149721
hg18149721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3059n100
Supporting Variantsnssv3559965
Samples
Known GenesFAM92B, KIAA0513, LOC400548
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063064
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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