A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874455



Internal ID22649407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:194316108..194327584hg38UCSC Ensembl
chr1:194285238..194296714hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3811477
hg1911477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874455
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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