A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574941



Internal ID20948012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177485474..177489723hg38UCSC Ensembl
chr3:177203262..177207511hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384250
hg194250
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263327
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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