A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573185



Internal ID20946256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144151272..144155248hg38UCSC Ensembl
chr6:144472409..144476385hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383977
hg193977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273169
Samples
Known GenesSTX11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573185
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