A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632620



Internal ID21824667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66469514..66473605hg38UCSC Ensembl
chr16:66503417..66507508hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384092
hg194092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038610
Supporting Variants
Samples
Known GenesBEAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632620
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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