A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261816



Internal ID20828856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181906980..181907450hg38UCSC Ensembl
chr3:181624768..181625238hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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