A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938430



Internal ID22713810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74098141..74098256hg38UCSC Ensembl
chr14:74564844..74564959hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375213
Samples
Known GenesLIN52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938430
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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