A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573954



Internal ID20947025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69111599..69112304hg38UCSC Ensembl
chr5:68407426..68408131hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266988
Samples
Known GenesSLC30A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573954
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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