A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17056720



Internal ID105645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46237378..46238290hg38UCSC Ensembl
chr12:46631161..46632073hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497434
Supporting Variants
Samples
Known GenesSLC38A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17056720
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.019513


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