A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574786



Internal ID21766829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138437337..138437337hg38UCSC Ensembl
chr6:138758474..138758474hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064515
Supporting Variants
Samples
Known GenesNHSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574786
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