A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794406



Internal ID21239744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24473741..24473741hg38UCSC Ensembl
chr14:24942947..24942947hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794406
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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