A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577057



Internal ID20950128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52680987..52681406hg38UCSC Ensembl
chr13:53255122..53255541hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224841
Samples
Known GenesSUGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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