A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598856



Internal ID21790901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71076018..71076018hg38UCSC Ensembl
chr14:71542735..71542735hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091842
Supporting Variants
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598856
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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