A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565262



Internal ID20938333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4594115..4594863hg38UCSC Ensembl
chr5:4594228..4594976hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565262
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