A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443584



Internal ID22501454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98012014..98012139hg38UCSC Ensembl
chr9:100774296..100774421hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911662
Supporting Variants
Samples
Known GenesANP32B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443584
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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