A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260017



Internal ID20827057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38288871..38294468hg38UCSC Ensembl
chr3:38330362..38335959hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg385598
hg195598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260017
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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