A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511316



Internal ID20884643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64891399..64891656hg38UCSC Ensembl
chr16:64925302..64925559hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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