A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431660



Internal ID22489530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28445840..28514682hg38UCSC Ensembl
chr7:28485458..28554300hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3868843
hg1968843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916564
Supporting Variants
Samples
Known GenesCREB5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431660
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01


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