A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586499



Internal ID21778542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76718954..76718954hg38UCSC Ensembl
chr11:76429998..76429998hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097606
Supporting Variants
Samples
Known GenesGUCY2EP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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