A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132933



Internal ID20699973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81886660..81887002hg38UCSC Ensembl
chr5:81182479..81182821hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.72795


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