A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233305



Internal ID20800345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14222225..14223139hg38UCSC Ensembl
chr12:14375159..14376073hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233305
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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