A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592096



Internal ID20965167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94562921..94563658hg38UCSC Ensembl
chr13:95215175..95215912hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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