A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912818



Internal ID22688034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16359635..16391461hg38UCSC Ensembl
chr9:16359633..16391459hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3831827
hg1931827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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