A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567455



Internal ID20940526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115173910..115174247hg38UCSC Ensembl
chr3:114892757..114893094hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567455
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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