A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457993



Internal ID236027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93035857..93044758hg38UCSC Ensembl
chr6:93745575..93754476hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg388902
hg198902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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