A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999028



Internal ID20566068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39809993..39823210hg38UCSC Ensembl
chr12:40203795..40217012hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3813218
hg1913218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474278
Supporting Variants
Samples
Known GenesSLC2A13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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