A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938437



Internal ID22713817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86890414..86908792hg38UCSC Ensembl
chr14:87356758..87375136hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3818379
hg1918379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379217
Samples
Known GenesLOC283585
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938437
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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