A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763659



Internal ID20539519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11514163..11514163hg38UCSC Ensembl
chr10:11556162..11556162hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267596
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763659
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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