A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229169



Internal ID20796209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22653153..22653387hg38UCSC Ensembl
chr12:22806087..22806321hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587091
Supporting Variants
Samples
Known GenesETNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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