A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570406



Internal ID21762449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38902701..38902701hg38UCSC Ensembl
chr6:38870477..38870477hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080352
Supporting Variants
Samples
Known GenesDNAH8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570406
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