A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922266



Internal ID22697491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105665102..105665378hg38UCSC Ensembl
chr9:108427383..108427659hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922266
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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