A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456862



Internal ID234920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141498762..141507699hg38UCSC Ensembl
chr6:141819899..141828836hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg388938
hg198938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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