A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627126



Internal ID21575431
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 Variantsnssv17068517
SamplesHG00731
Known GenesGUCY2GP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627126
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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