A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220606



Internal ID20787646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41964993..41965119hg38UCSC Ensembl
chr13:42539129..42539255hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579377
Supporting Variants
Samples
Known GenesVWA8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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