A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416921



Internal ID22474791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96819229..96834065hg38UCSC Ensembl
chr4:97740380..97755216hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3814837
hg1914837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416921
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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