A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515368



Internal ID20888727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:622106..656924hg38UCSC Ensembl
chr16:672106..706924hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3834819
hg1934819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177302
Samples
Known GenesC16orf13, FAM195A, RAB40C, WDR90, WFIKKN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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