A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570423



Internal ID20943494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138613690..138614287hg38UCSC Ensembl
chr3:138332532..138333129hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259716
Samples
Known GenesFAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570423
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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