A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576070



Internal ID20949141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75576345..75577051hg38UCSC Ensembl
chr13:76150481..76151187hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219791
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576070
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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