A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983697



Internal ID56508
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 StatusS
Merged Variantsnsv5458331
Supporting Variants
Samples
Known GenesGLP1R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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