A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928619



Internal ID22703861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71411338..71418087hg38UCSC Ensembl
chr14:71878055..71884804hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg386750
hg196750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928619
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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