A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245218



Internal ID20812258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51226762..51227254hg38UCSC Ensembl
chr17:49304123..49304615hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576608
Supporting Variants
Samples
Known GenesMBTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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