A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937703



Internal ID22713075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48573124..48588351hg38UCSC Ensembl
chr14:49042327..49057554hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3815228
hg1915228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937703
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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