A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586710



Internal ID20959781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20360612..20775569hg38UCSC Ensembl
chr13:20934751..21349708hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38414958
hg19414958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233300
Samples
Known GenesCRYL1, IFT88, IL17D, MIR4499, N6AMT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586710
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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