A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573469



Internal ID20946540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125416091..125416805hg38UCSC Ensembl
chr3:125134935..125135649hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573469
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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