A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445846



Internal ID22503716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140481786..140489419hg38UCSC Ensembl
chr7:140181586..140189219hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg387634
hg197634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445846
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.220


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