A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461043



Internal ID239008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10096808..10105220hg38UCSC Ensembl
chr6:10097041..10105453hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg388413
hg198413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461043
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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