A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218107



Internal ID20785147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102832983..102833620hg38UCSC Ensembl
chr13:103485333..103485970hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594294
Supporting Variants
Samples
Known GenesBIVM, BIVM-ERCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218107
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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