A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441155



Internal ID22499025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4710326..4909311hg38UCSC Ensembl
chr9:4710326..4909311hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38198986
hg19198986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911032
Supporting Variants
Samples
Known GenesAK3, MIR101-2, RCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441155
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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