A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525117



Internal ID301292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9881382..9881675hg38UCSC Ensembl
chr17:9784699..9784992hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711364
Samples
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525117
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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