A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893464



Internal ID22668524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27892547..27892671hg38UCSC Ensembl
chr6:27860325..27860449hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893464
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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