A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555319



Internal ID328478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110124488..110124539hg38UCSC Ensembl
chr10:111884246..111884297hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041042
Samples
Known GenesADD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555319
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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