A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762981



Internal ID20538841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71045663..71045663hg38UCSC Ensembl
chr17:69041804..69041804hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762981
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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