A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260555



Internal ID20827595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172504214..172504822hg38UCSC Ensembl
chr3:172222004..172222612hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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