A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585562



Internal ID20958633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27733057..27733941hg38UCSC Ensembl
chr13:28307194..28308078hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1786n223
Supporting Variantsnssv18230888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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