A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233403



Internal ID20800443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51014096..51014867hg38UCSC Ensembl
chr12:51407879..51408650hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576535
Supporting Variants
Samples
Known GenesSLC11A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233403
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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