A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227884



Internal ID20794924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95748191..95748714hg38UCSC Ensembl
chr12:96141969..96142492hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590520
Supporting Variants
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00034


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