A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5402806



Internal ID182172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96305773..96305824hg38UCSC Ensembl
chr5:95641477..95641528hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5402806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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