A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127590



Internal ID20694630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164294921..167231615hg38UCSC Ensembl
chr5:163721927..166658620hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382936695
hg192936694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399128
Supporting Variants
Samples
Known GenesLOC101927835, LOC102546299, LOC102557615
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127590
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