A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560664



Internal ID20933735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34921025..34921870hg38UCSC Ensembl
chr5:34921130..34921975hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268229
Samples
Known GenesBRIX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560664
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