A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501181



Internal ID20874412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85987523..85989529hg38UCSC Ensembl
chr16:86021129..86023135hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382007
hg192007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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