A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260036



Internal ID20827076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31846145..31847210hg38UCSC Ensembl
chr2:32071214..32072279hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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