A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757687



Internal ID20533547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112331824..112331824hg38UCSC Ensembl
chr11:112202547..112202547hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757687
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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