A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223632



Internal ID20790672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101483660..101484534hg38UCSC Ensembl
chr12:101877438..101878312hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592831
Supporting Variants
Samples
Known GenesSPIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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