A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410968



Internal ID22468838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142922054..142998827hg38UCSC Ensembl
chr4:143843207..143919980hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3876774
hg1976774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410968
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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