A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219861



Internal ID20786901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95053963..95055756hg38UCSC Ensembl
chr12:95447739..95449532hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590897
Supporting Variants
Samples
Known GenesNR2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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