A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610699



Internal ID21802746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25112545..25112545hg38UCSC Ensembl
chr14:25581751..25581751hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610699
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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