A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900083



Internal ID22675222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152905617..152906603hg38UCSC Ensembl
chr6:153226752..153227738hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900083
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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