A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764697



Internal ID20540557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64377511..64377511hg38UCSC Ensembl
chr11:64144983..64144983hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764697
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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