A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514367



Internal ID20887720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4286673..4291475hg38UCSC Ensembl
chr16:4336674..4341476hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384803
hg194803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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