A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140912



Internal ID20707952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145064421..145065096hg38UCSC Ensembl
chr6:145385557..145386232hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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