A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903269



Internal ID22678435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157275699..157275980hg38UCSC Ensembl
chr6:157696731..157697012hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903269
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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