A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509890



Internal ID20883203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5438379..5510341hg38UCSC Ensembl
chr16:5488380..5560342hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3871963
hg1971963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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