A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510581



Internal ID20883901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69387912..69390270hg38UCSC Ensembl
chr16:69421815..69424173hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382359
hg192359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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