A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916976



Internal ID22692195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98238007..98238825hg38UCSC Ensembl
chr9:101000289..101001107hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443283
Samples
Known GenesTBC1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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