A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897417



Internal ID22672519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128573650..128573931hg38UCSC Ensembl
chr6:128894795..128895076hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897417
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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