A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437762



Internal ID22495632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45464575..45465872hg38UCSC Ensembl
chr7:45504174..45505471hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437762
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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