A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871469



Internal ID22646407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219312629..219325711hg38UCSC Ensembl
chr1:219485971..219499053hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3813083
hg1913083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871469
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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