A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919628



Internal ID22694850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33423085..33424832hg38UCSC Ensembl
chr9:33423083..33424830hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2100n209
Supporting Variantsnssv17438749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919628
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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