A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234354



Internal ID20801395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48673040..48673252hg38UCSC Ensembl
chr12:49066823..49067035hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575956
Supporting Variants
Samples
Known GenesKANSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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