A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219214



Internal ID20786254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42903987..43318020hg38UCSC Ensembl
chr13:43478123..43892156hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38414034
hg19414034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577207
Supporting Variants
Samples
Known GenesDNAJC15, ENOX1, EPSTI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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