A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003326



Internal ID69835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137461761..137467694hg38UCSC Ensembl
chr7:137146507..137152440hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg385934
hg195934
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562598
Supporting Variants
Samples
Known GenesDGKI
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003326
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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