A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144873



Internal ID344078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66789290..66789624hg38UCSC Ensembl
chr16:66823193..66823527hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709115
Samples
Known GenesCCDC79
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144873
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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