A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613242



Internal ID21805289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93961239..93962111hg38UCSC Ensembl
chr14:94427585..94428457hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023157
Supporting Variants
Samples
Known GenesASB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613242
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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