A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768102



Internal ID20543962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16564733..16564733hg38UCSC Ensembl
chr21:17937053..17937053hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285701
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768102
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