A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067532



Internal ID21478882
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 StatusS
Merged Variantsnsv5629134
Supporting Variants
SamplesHG03486
Known GenesGFRA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067532
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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