A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934094



Internal ID22709414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63165106..63523889hg38UCSC Ensembl
chr14:63631824..63990607hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38358784
hg19358784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384818
Samples
Known GenesGPHB5, PPP2R5E, RHOJ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934094
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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