A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579009



Internal ID20952080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44892688..44893261hg38UCSC Ensembl
chr13:45466823..45467396hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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