A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947134



Internal ID22722636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34695819..34697383hg38UCSC Ensembl
chr14:35165025..35166589hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947134
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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