A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944523



Internal ID21364592
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 Variantsnssv15176123
SamplesHG002
Known GenesCCDC79
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944523
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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