A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139781



Internal ID20706821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155396790..155397420hg38UCSC Ensembl
chr6:155717924..155718554hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609251
Supporting Variants
Samples
Known GenesNOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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