A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126892



Internal ID20693932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159614695..159618178hg38UCSC Ensembl
chr5:159041702..159045185hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383484
hg193484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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