A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499197



Internal ID20872414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62882718..62992899hg38UCSC Ensembl
chr16:62916622..63026803hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38110182
hg19110182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499197
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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