A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755769



Internal ID20531629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865750..131865750hg38UCSC Ensembl
chr11:131735644..131735644hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276138
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755769
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer