A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547338



Internal ID20920541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98586030..98586662hg38UCSC Ensembl
chr3:98304874..98305506hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262764
Samples
Known GenesCPOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547338
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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