A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530293



Internal ID306284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57535703..57535780hg38UCSC Ensembl
chr16:57569615..57569692hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709481
Samples
Known GenesCCDC102A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530293
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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