A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760566



Internal ID20536426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30237264..30237264hg38UCSC Ensembl
chr17:28564282..28564282hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760566
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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