A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217502



Internal ID20784542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32847966..32848721hg38UCSC Ensembl
chr13:33422104..33422859hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581056
Supporting Variants
Samples
Known GenesLINC00423
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217502
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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