A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943505



Internal ID22718954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59247621..59247699hg38UCSC Ensembl
chr16:59281525..59281603hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943505
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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