A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501687



Internal ID20874924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67514089..67527162hg38UCSC Ensembl
chr16:67547992..67561065hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3813074
hg1913074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031362
Samples
Known GenesLOC100505942
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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