A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559318



Internal ID21883673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137648100..137648194hg38UCSC Ensembl
chr6:137969237..137969331hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103847
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559318
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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