A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587069



Internal ID20960140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28133379..28134063hg38UCSC Ensembl
chr13:28707516..28708200hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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