A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459484



Internal ID237499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90024787..90024883hg38UCSC Ensembl
chr6:90734506..90734602hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985396
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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