A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233955



Internal ID20800996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119843764..119844142hg38UCSC Ensembl
chr12:120281568..120281946hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584216
Supporting Variants
Samples
Known GenesCIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233955
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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