A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508812



Internal ID20882116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20328052..20336094hg38UCSC Ensembl
chr16:20339374..20347416hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg388043
hg198043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028367
Samples
Known GenesUMOD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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