A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566181



Internal ID21758224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127482331..127482572hg38UCSC Ensembl
chr6:127803476..127803717hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003544
Supporting Variants
Samples
Known GenesSOGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566181
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