A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552293



Internal ID21876648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63877166..63877166hg38UCSC Ensembl
chr3:63862842..63862842hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070220
Supporting Variants
Samples
Known GenesATXN7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552293
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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