A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506044



Internal ID20879319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81386316..81394315hg38UCSC Ensembl
chr16:81419921..81427920hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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