A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940109



Internal ID22715513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57486753..57486821hg38UCSC Ensembl
chr16:57520665..57520733hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940109
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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