A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232988



Internal ID20800028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111735062..111735640hg38UCSC Ensembl
chr12:112172866..112173444hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579554
Supporting Variants
Samples
Known GenesACAD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00033


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