A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472789



Internal ID250492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152835235..152853294hg38UCSC Ensembl
chr6:153156370..153174429hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3818060
hg1918060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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