A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514151



Internal ID20887503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81744146..81772032hg38UCSC Ensembl
chr16:81777751..81805637hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3827887
hg1927887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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