A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591180



Internal ID20964251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25752451..25753296hg38UCSC Ensembl
chr15:25997598..25998443hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2467n223
Supporting Variantsnssv18239399
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591180
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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