A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403299



Internal ID182662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95635467..95635467hg38UCSC Ensembl
chr7:95264779..95264779hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403299
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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