A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234406



Internal ID20801446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43793838..43794020hg38UCSC Ensembl
chr13:44367974..44368156hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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