A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561627



Internal ID21885982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3092622..3093135hg38UCSC Ensembl
chr6:3092856..3093369hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000559
Supporting Variants
Samples
Known GenesRIPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561627
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