A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218305



Internal ID20785345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49057690..49063563hg38UCSC Ensembl
chr13:49631826..49637699hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385874
hg195874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590240
Supporting Variants
Samples
Known GenesFNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218305
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00051


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