A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608182



Internal ID21800229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96305003..96305003hg38UCSC Ensembl
chr14:96771340..96771340hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091631
Supporting Variants
Samples
Known GenesATG2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608182
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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