A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735284



Internal ID158950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140493877..140801056hg38UCSC Ensembl
chr6:140815014..141122193hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38307180
hg19307180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457536
Supporting Variants
Samples
Known GenesMIR4465
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735284
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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