A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561608



Internal ID21885963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134213546..134213629hg38UCSC Ensembl
chr6:134534684..134534767hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002610
Supporting Variants
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561608
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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