A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5394488



Internal ID173919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60026252..60026303hg38UCSC Ensembl
chr10:61786010..61786061hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035872
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5394488
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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