A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229236



Internal ID20796276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98596965..98597465hg38UCSC Ensembl
chr12:98990743..98991243hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591260
Supporting Variants
Samples
Known GenesSLC25A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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