A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235437



Internal ID20802477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10905307..10906529hg38UCSC Ensembl
chr12:11057906..11059128hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586016
Supporting Variants
Samples
Known GenesPRH1-PRR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235437
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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