A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147038



Internal ID346244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4979122..4988863hg38UCSC Ensembl
chr10:5021314..5031055hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg389742
hg199742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683702
Samples
Known GenesAKR1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147038
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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