A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591981



Internal ID20965052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66540448..66540791hg38UCSC Ensembl
chr15:66832786..66833129hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2570n223
Supporting Variantsnssv18238952
Samples
Known GenesZWILCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591981
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