A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941245



Internal ID22716666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67515598..67515649hg38UCSC Ensembl
chr14:67982315..67982366hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941245
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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