A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711364



Internal ID135030
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 StatusS
Merged Variantsnsv5525117
Supporting Variants
Samples
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711364
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.071495


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