A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218132



Internal ID20785172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110210740..110210949hg38UCSC Ensembl
chr12:110648545..110648754hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575895
Supporting Variants
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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