A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610063



Internal ID21802110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4700423..4720181hg38UCSC Ensembl
chr16:4750424..4770182hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819759
hg1919759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037072
Supporting Variants
Samples
Known GenesANKS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610063
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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