A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756805



Internal ID20532665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75763437..75763437hg38UCSC Ensembl
chr11:75474482..75474482hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281341
Samples
Known GenesLOC283214
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756805
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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