A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515228



Internal ID20888587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4305001..4308800hg38UCSC Ensembl
chr16:4355002..4358801hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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