A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748707



Internal ID20524734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116841755..116842068hg38UCSC Ensembl
chr11:116712471..116712784hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748707
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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