A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504446



Internal ID20877707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80261114..80319108hg38UCSC Ensembl
chr16:80295011..80353005hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3857995
hg1957995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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