A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263239



Internal ID20830279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152870337..152876028hg38UCSC Ensembl
chr3:152588126..152593817hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg385692
hg195692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263239
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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