A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606955



Internal ID21799002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72785143..72785143hg38UCSC Ensembl
chr14:73251851..73251851hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383717
hg193717
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085532
Supporting Variants
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606955
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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