A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230436



Internal ID20797476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1667780..1667890hg38UCSC Ensembl
chr12:1776946..1777056hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230436
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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