A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881851



Internal ID22656827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110929262..110931480hg38UCSC Ensembl
chr1:111471884..111474102hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382219
hg192219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881851
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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