A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504782



Internal ID20878045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19649703..19764765hg38UCSC Ensembl
chr16:19661025..19776087hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38115063
hg19115063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180035
Samples
Known GenesC16orf62, IQCK, KNOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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