A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756971



Internal ID20532831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80242550..80242550hg38UCSC Ensembl
chr16:80276447..80276447hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756971
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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