A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905778



Internal ID22680970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112006258..112008700hg38UCSC Ensembl
chr6:112327461..112329903hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382443
hg192443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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