A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493458



Internal ID22551387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3057761..3061676hg38UCSC Ensembl
chr4:3059488..3063403hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383916
hg193916
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493458
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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