A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751207



Internal ID20527067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56739255..56739255hg38UCSC Ensembl
chr16:56773167..56773167hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273680
Samples
Known GenesNUP93
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751207
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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