A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552958



Internal ID20926076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49364425..49365436hg38UCSC Ensembl
chr3:49401858..49402869hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262816
Samples
Known GenesRHOA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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