A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752898



Internal ID20528758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72236597..72236597hg38UCSC Ensembl
chr17:70232738..70232738hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752898
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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