A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765637



Internal ID20541497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56993092..56993092hg38UCSC Ensembl
chr16:57027004..57027004hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765637
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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