A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921769



Internal ID22696993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105112650..105113349hg38UCSC Ensembl
chr9:107874931..107875630hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921769
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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