A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122329



Internal ID20689369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107772275..107772853hg38UCSC Ensembl
chr5:107107976..107108554hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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