A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507795



Internal ID20881091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86522069..86522334hg38UCSC Ensembl
chr16:86555675..86555940hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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