A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755186



Internal ID20531046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65676392..65676392hg38UCSC Ensembl
chr11:65443863..65443863hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755186
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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