A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765544



Internal ID20541404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34480609..34480609hg38UCSC Ensembl
chr17:32807628..32807628hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765544
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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