A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950061



Internal ID22668287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112314099..112314099hg38UCSC Ensembl
chr10:114073857..114073857hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367687
Samples
Known GenesGUCY2GP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950061
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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