A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580982



Internal ID20954053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28272581..28273467hg38UCSC Ensembl
chr13:28846718..28847604hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229113
Samples
Known GenesPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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