A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494490



Internal ID22552421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38717983..38727020hg38UCSC Ensembl
chr4:38719604..38728641hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg389038
hg199038
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494490
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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