A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559308



Internal ID20932379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67347331..67348509hg38UCSC Ensembl
chr4:68213049..68214227hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559308
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