A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584480



Internal ID20957551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88522724..88523764hg38UCSC Ensembl
chr13:89174979..89176019hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg381041
hg191041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1955n223
Supporting Variantsnssv18220843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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