A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748315



Internal ID20524340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66460044..66460368hg38UCSC Ensembl
chr11:66227515..66227839hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748315
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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