A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578043



Internal ID20951114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94547728..94556911hg38UCSC Ensembl
chr13:95199982..95209165hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg389184
hg199184
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578043
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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