A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763443



Internal ID20539303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28223957..28223957hg38UCSC Ensembl
chr17:26550983..26550983hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763443
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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