A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514311



Internal ID20887663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1336430..1451010hg38UCSC Ensembl
chr16:1386431..1501011hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38114581
hg19114581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193205
Samples
Known GenesBAIAP3, C16orf91, CCDC154, CLCN7, GNPTG, TSR3, UNKL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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