A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260492



Internal ID20827532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170188570..170189224hg38UCSC Ensembl
chr3:169906358..169907012hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568490
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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