A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135389



Internal ID20702430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110995025..110997628hg38UCSC Ensembl
chr6:111316228..111318831hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382604
hg192604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601218
Supporting Variants
Samples
Known GenesRPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135389
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