A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217895



Internal ID20784935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45753085..45753701hg38UCSC Ensembl
chr12:46146868..46147484hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578223
Supporting Variants
Samples
Known GenesARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217895
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00028


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