A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553517



Internal ID21877872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115664230..115664230hg38UCSC Ensembl
chr3:115383077..115383077hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078505
Supporting Variants
Samples
Known GenesGAP43
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553517
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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