A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497683



Internal ID20870891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74977485..74988565hg38UCSC Ensembl
chr16:75011383..75022463hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3811081
hg1911081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178552
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497683
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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