A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100456



Internal ID21489139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9879291..9879291hg38UCSC Ensembl
chr17:9782608..9782608hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647376
Supporting Variants
SamplesNA18939
Known GenesGLP2R
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100456
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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