A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382852



Internal ID22440722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24473724..24473724hg38UCSC Ensembl
chr14:24942930..24942930hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382852
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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