A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500159



Internal ID277101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104814327..104814446hg38UCSC Ensembl
chr12:105208105..105208224hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690544
Samples
Known GenesSLC41A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500159
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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