A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411320



Internal ID22469190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:93126436..93190682hg38UCSC Ensembl
chr4:94047587..94111833hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3864247
hg1964247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895639
Supporting Variants
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411320
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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