A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890033



Internal ID22665057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121474423..121479199hg38UCSC Ensembl
chr6:121795569..121800345hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384777
hg194777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890033
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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