A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500458



Internal ID20873685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34213201..34273300hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3860100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500458
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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