A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554676



Internal ID327854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69213578..69213629hg38UCSC Ensembl
chr10:70973334..70973385hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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