A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414959



Internal ID21072512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159466301..159472100hg38UCSC Ensembl
chr5:158893309..158899108hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414959
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