A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939377



Internal ID22714770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102934273..102934749hg38UCSC Ensembl
chr14:103400610..103401086hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385837
Samples
Known GenesCDC42BPB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939377
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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