A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942767



Internal ID22718209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24598815..24599704hg38UCSC Ensembl
chr14:25068021..25068910hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942767
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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