A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136044



Internal ID20703084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86675901..86677400hg38UCSC Ensembl
chr5:85971718..85973217hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136044
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