A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580056



Internal ID20953127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20655338..20655581hg38UCSC Ensembl
chr13:21229477..21229720hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233791
Samples
Known GenesIFT88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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