A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258449



Internal ID20825489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80962564..83437056hg38UCSC Ensembl
chr2:81189688..83664180hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg382474493
hg192474493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551157
Supporting Variants
Samples
Known GenesLOC1720
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258449
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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