A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505326



Internal ID20878594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58800813..58817261hg38UCSC Ensembl
chr16:58834717..58851165hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3816449
hg1916449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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