A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869222



Internal ID22644157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214708844..214708909hg38UCSC Ensembl
chr1:214882187..214882252hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869222
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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