A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932742



Internal ID22708045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15089543..15098620hg38UCSC Ensembl
chr16:15183400..15192477hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg389078
hg199078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381656
Samples
Known GenesPDXDC1, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932742
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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