A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218236



Internal ID20785276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40993743..40994373hg38UCSC Ensembl
chr13:41567879..41568509hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584521
Supporting Variants
Samples
Known GenesELF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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