A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495698



Internal ID20868892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86317928..86326152hg38UCSC Ensembl
chr16:86351534..86359758hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg388225
hg198225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2958n223
Supporting Variantsnssv18033472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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