A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913288



Internal ID22688504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10633431..10634294hg38UCSC Ensembl
chr9:10633431..10634294hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913288
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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