A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923722



Internal ID22698949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4406089..4443715hg38UCSC Ensembl
chr9:4406089..4443715hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3837627
hg1937627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923722
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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