A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884193



Internal ID22659175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244348581..244348846hg38UCSC Ensembl
chr1:244511883..244512148hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884193
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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