A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539518



Internal ID20912813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42208952..42209446hg38UCSC Ensembl
chr21:43629062..43629556hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072456
Samples
Known GenesABCG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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