A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564908



Internal ID20937979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97722087..98024523hg38UCSC Ensembl
chr5:97057791..97360227hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38302437
hg19302437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564908
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