A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567739



Internal ID20940810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189846708..189847288hg38UCSC Ensembl
chr3:189564497..189565077hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5128n223
Supporting Variantsnssv18261887
Samples
Known GenesTP63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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