A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260073



Internal ID20827113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32261330..32262087hg38UCSC Ensembl
chr2:32486399..32487156hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540659
Supporting Variants
Samples
Known GenesNLRC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260073
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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