A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145653



Internal ID344858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66759497..66760113hg38UCSC Ensembl
chr16:66793400..66794016hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709113
Samples
Known GenesCCDC79
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145653
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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