A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888300



Internal ID22663304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154908626..154944688hg38UCSC Ensembl
chr6:155229760..155265822hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3836063
hg1936063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888300
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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