A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443871



Internal ID22501741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95986751..95986808hg38UCSC Ensembl
chr7:95616063..95616120hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918409
Supporting Variants
Samples
Known GenesDYNC1I1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443871
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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