A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756732



Internal ID20532592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74139955..74139955hg38UCSC Ensembl
chr11:73851000..73851000hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266460
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756732
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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