A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415388



Internal ID22473258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11545953..11617470hg38UCSC Ensembl
chr4:11547577..11619094hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3871518
hg1971518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415388
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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