A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583256



Internal ID20956327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40747680..40748454hg38UCSC Ensembl
chr13:41321816..41322590hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220125
Samples
Known GenesMRPS31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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