A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945993



Internal ID22721477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49955557..49956482hg38UCSC Ensembl
chr16:49989468..49990393hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945993
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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