A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063360



Internal ID19152579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88386848..88424550hg38UCSC Ensembl
Innerchr16:88453256..88490958hg19UCSC Ensembl
Innerchr16:86980757..87018459hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3837703
hg1937703
hg1837703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3063n100
Supporting Variantsnssv3559989
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063360
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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