A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748431



Internal ID20524456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7980819..7980926hg38UCSC Ensembl
chr11:8002366..8002473hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748431
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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