A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218061



Internal ID20785101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42490840..42491421hg38UCSC Ensembl
chr12:42884642..42885223hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581826
Supporting Variants
Samples
Known GenesPRICKLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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