A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565135



Internal ID21889490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163611861..163611861hg38UCSC Ensembl
chr6:164032893..164032893hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565135
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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