A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384154



Internal ID21041707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16946443..16954565hg38UCSC Ensembl
chr5:16946552..16954674hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg388123
hg198123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer