A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140084



Internal ID20707124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22640381..22645932hg38UCSC Ensembl
chr6:22640610..22646161hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385552
hg195552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140084
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