A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944511



Internal ID22719977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56712036..56732249hg38UCSC Ensembl
chr14:57178754..57198967hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3820214
hg1920214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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