A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585416



Internal ID20958487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60149631..60150150hg38UCSC Ensembl
chr13:60723765..60724284hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219035
Samples
Known GenesDIAPH3, DIAPH3-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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