A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500446



Internal ID20873673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85448297..85449040hg38UCSC Ensembl
chr16:85481903..85482646hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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