A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443918



Internal ID22501788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109041531..109042912hg38UCSC Ensembl
chr9:111803811..111805192hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381382
hg191382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916849
Supporting Variants
Samples
Known GenesTMEM245
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443918
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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