A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497575



Internal ID20870782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68977747..68979167hg38UCSC Ensembl
chr16:69011650..69013070hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381421
hg191421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031752
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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