A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140677



Internal ID20707717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24984701..24988100hg38UCSC Ensembl
chr6:24984929..24988328hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405498
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140677
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