A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585861



Internal ID20958932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79377700..79378270hg38UCSC Ensembl
chr13:79951835..79952405hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229615
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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