A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384525



Internal ID21042078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145484982..145485597hg38UCSC Ensembl
chr4:146406134..146406749hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108884
Samples
Known GenesSMAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384525
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