A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560182



Internal ID20933253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69107813..69108579hg38UCSC Ensembl
chr5:68403640..68404406hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266986
Samples
Known GenesSLC30A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560182
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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