A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933457



Internal ID22708770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85734693..85738551hg38UCSC Ensembl
chr14:86201037..86204895hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933457
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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