A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504399



Internal ID20877660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5995815..6002950hg38UCSC Ensembl
chr16:6045816..6052951hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387136
hg197136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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