A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626234



Internal ID21818281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9879291..9879291hg38UCSC Ensembl
chr17:9782608..9782608hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083811
Supporting Variants
Samples
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626234
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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