A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260061



Internal ID20827101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32150951..32151912hg38UCSC Ensembl
chr2:32376020..32376981hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553475
Supporting Variants
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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