A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756928



Internal ID20532788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95095424..95095424hg38UCSC Ensembl
chr11:94828588..94828588hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287475
Samples
Known GenesENDOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756928
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