A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564602



Internal ID20937673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173146383..173148049hg38UCSC Ensembl
chr4:174067534..174069200hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564602
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