A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555118



Internal ID20928207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32338128..32339959hg38UCSC Ensembl
chr3:32379620..32381451hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381832
hg191832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261381
Samples
Known GenesCMTM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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