A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735662



Internal ID20511606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4719886..4722305hg38UCSC Ensembl
chr16:4769887..4772306hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382420
hg192420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287567
Samples
Known GenesANKS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735662
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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