A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112255



Internal ID22021490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26591396..26936371hg38UCSC Ensembl
chr10:26880325..27225300hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38344976
hg19344976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587383
Samples
Known GenesABI1, LINC00202-1, LINC00202-2, LINC00264, PDSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112255
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