A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260237



Internal ID20827277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39451275..39482580hg38UCSC Ensembl
chr2:39678416..39709721hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3831306
hg1931306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543593
Supporting Variants
Samples
Known GenesLOC728730
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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