A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889086



Internal ID22664098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26611010..26617790hg38UCSC Ensembl
chr6:26611238..26618018hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386781
hg196781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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