A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107250



Internal ID22016483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36663036..36663036hg38UCSC Ensembl
chr20:35291439..35291439hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633207
Samples
Known GenesNDRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107250
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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