A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027000



Internal ID21936343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66789290..66789625hg38UCSC Ensembl
chr16:66823193..66823528hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619932
Samples
Known GenesCCDC79
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027000
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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