A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746189



Internal ID20522200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27473914..27474124hg38UCSC Ensembl
chr6:27441693..27441903hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746189
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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