A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127365



Internal ID20694405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166217601..166219200hg38UCSC Ensembl
chr5:165644606..165646205hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127365
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