A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606928



Internal ID21798975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57041272..57041272hg38UCSC Ensembl
chr14:57507990..57507990hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606928
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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