A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218763



Internal ID20785803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118384708..118385203hg38UCSC Ensembl
chr12:118822513..118823008hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585344
Supporting Variants
Samples
Known GenesSUDS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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