A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230983



Internal ID20798023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48669572..48669967hg38UCSC Ensembl
chr12:49063355..49063750hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591845
Supporting Variants
Samples
Known GenesKANSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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