A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226708



Internal ID20793748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91493366..91496629hg38UCSC Ensembl
chr13:92145620..92148883hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg383264
hg193264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584851
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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