A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583897



Internal ID20956968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128057384..128060574hg38UCSC Ensembl
chr10:129855648..129858838hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383191
hg193191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224165
Samples
Known GenesPTPRE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583897
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