A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283360



Internal ID20492578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115664237..115664237hg38UCSC Ensembl
chr3:115383084..115383084hg19UCSC 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 Variantsnsv4758117
Supporting Variants
Samples
Known GenesGAP43
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283360
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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