A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586323



Internal ID20959394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31452497..31453808hg38UCSC Ensembl
chr13:32026634..32027945hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1792n223
Supporting Variantsnssv18231092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586323
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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