A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505338



Internal ID20878607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71412826..71476729hg38UCSC Ensembl
chr16:71446729..71510632hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3863904
hg1963904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188424
Samples
Known GenesZNF19, ZNF23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505338
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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