A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262661



Internal ID20829701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45564936..45568994hg38UCSC Ensembl
chr3:45606428..45610486hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384059
hg194059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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