A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937831



Internal ID22713204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25466026..25466742hg38UCSC Ensembl
chr16:25477347..25478063hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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