A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588667



Internal ID20961738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40694069..40694873hg38UCSC Ensembl
chr13:41268205..41269009hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1809n223
Supporting Variantsnssv18221019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer