A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458331



Internal ID236361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39049994..39052523hg38UCSC Ensembl
chr6:39017770..39020299hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382530
hg192530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983697
Samples
Known GenesGLP1R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458331
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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