A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021509



Internal ID21930852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66380154..66380219hg38UCSC Ensembl
chr16:66414057..66414122hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618409
Samples
Known GenesCDH5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021509
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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