A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947026



Internal ID22722526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71183750..71183845hg38UCSC Ensembl
chr14:71650467..71650562hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947026
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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