A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559965



Internal ID18511560
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 StatusS
Merged Variantsnsv1063064
Supporting Variants
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)nssv3559965
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer