A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261887



Internal ID20828927
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 StatusS
Merged Variantsnsv6567739
Supporting Variants
Samples
Known GenesTP63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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