A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586416



Internal ID20959487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34506139..34508221hg38UCSC Ensembl
chr13:35080276..35082358hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg382083
hg192083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232383
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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