A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563898



Internal ID20936969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132547835..132549297hg38UCSC Ensembl
chr5:131883527..131884989hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381463
hg191463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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