A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990453



Internal ID61043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10197..16414hg38UCSC Ensembl
chr7:10197..16414hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg386218
hg196218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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