A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887094



Internal ID22662086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227861782..227877358hg38UCSC Ensembl
chr1:228049483..228065059hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3815577
hg1915577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887094
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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