A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565907



Internal ID21757872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163907502..163908610hg38UCSC Ensembl
chr6:164328534..164329642hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565907
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