A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869734



Internal ID22644669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244455754..244458434hg38UCSC Ensembl
chr1:244619056..244621736hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg382681
hg192681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869734
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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