A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375768



Internal ID22601437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9881368..9881674hg38UCSC Ensembl
chr17:9784685..9784991hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934794
Supporting Variants
Samples
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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