A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559629



Internal ID20932700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139272761..139273760hg38UCSC Ensembl
chr6:139593898..139594897hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272492
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559629
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