A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904228



Internal ID22679404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9460144..9460480hg38UCSC Ensembl
chr6:9460377..9460713hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904228
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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