A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437881



Internal ID216461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171007266..171008741hg38UCSC Ensembl
chr3:170725055..170726530hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941867
Samples
Known GenesSLC2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437881
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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