A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944107



Internal ID22719566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10150606..10151045hg38UCSC Ensembl
chr18:10150603..10151042hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv941n209
Supporting Variantsnssv17378469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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