A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931563



Internal ID22706849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21722773..21727986hg38UCSC Ensembl
chr14:22191020..22196260hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385214
hg195241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931563
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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