A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946492



Internal ID22721983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74103519..74131404hg38UCSC Ensembl
chr14:74570222..74598107hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827886
hg1927886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371339
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946492
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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