A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258877



Internal ID20825917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100800610..100800894hg38UCSC Ensembl
chr3:100519454..100519738hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547811
Supporting Variants
Samples
Known GenesABI3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258877
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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