A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999030



Internal ID20566070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39818125..39824314hg38UCSC Ensembl
chr12:40211927..40218116hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg386190
hg196190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456746
Supporting Variants
Samples
Known GenesSLC2A13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999030
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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