A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217572



Internal ID20784612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100481680..100483121hg38UCSC Ensembl
chr12:100875458..100876899hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587595
Supporting Variants
Samples
Known GenesNR1H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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