A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380259



Internal ID22438129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72866243..72867097hg38UCSC Ensembl
chr14:73332951..73333805hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943622
Supporting Variants
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380259
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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