A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576964



Internal ID20950035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91848845..91850371hg38UCSC Ensembl
chr10:93608602..93610128hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381527
hg191527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233187
Samples
Known GenesTNKS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576964
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