A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578254



Internal ID20951325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110624026..110624778hg38UCSC Ensembl
chr13:111276373..111277125hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230743
Samples
Known GenesCARKD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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