A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733739



Internal ID20509669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8953537..8953732hg38UCSC Ensembl
chr16:9047394..9047589hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271727
Samples
Known GenesUSP7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733739
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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