A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579784



Internal ID20952855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31841273..31841714hg38UCSC Ensembl
chr13:32415410..32415851hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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