A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592855



Internal ID20965926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44888810..44889342hg38UCSC Ensembl
chr13:45462945..45463477hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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