A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146065



Internal ID20713105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85649541..85652489hg38UCSC Ensembl
chr6:86359259..86362207hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg382949
hg192949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146065
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