A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553151



Internal ID20926260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32243041..32243546hg38UCSC Ensembl
chr3:32284533..32285038hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261376
Samples
Known GenesCMTM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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