A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568333



Internal ID20941404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43008707..43015509hg38UCSC Ensembl
chr4:43010724..43017526hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386803
hg196803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265667
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568333
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