A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941752



Internal ID22717182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63871601..63873967hg38UCSC Ensembl
chr16:63905505..63907871hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382367
hg192367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941752
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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