A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262467



Internal ID20829507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142482035..142482381hg38UCSC Ensembl
chr3:142200877..142201223hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568166
Supporting Variants
Samples
Known GenesATR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262467
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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