A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932815



Internal ID22708119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12605988..12624769hg38UCSC Ensembl
chr16:12699845..12718626hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3818782
hg1918782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932815
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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