A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919466



Internal ID22694688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90937725..90937804hg38UCSC Ensembl
chr9:93700007..93700086hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919466
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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