A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738330



Internal ID20514298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58993723..58994139hg38UCSC Ensembl
chr16:59027627..59028043hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738330
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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