A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735400



Internal ID20511342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59862144..59862287hg38UCSC Ensembl
chr16:59896048..59896191hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735400
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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