A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629134



Internal ID21577439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116064085..116064085hg38UCSC Ensembl
chr10:117823596..117823596hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067532
SamplesHG03486
Known GenesGFRA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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