A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097537



Internal ID22006770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113841478..113841478hg38UCSC Ensembl
chr13:114544451..114544451hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602036, nssv17611786
Samples
Known GenesGAS6, GAS6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097537
Frequency
Sample Size405
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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