A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535181



Internal ID310872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33545281..33545292hg38UCSC Ensembl
chr10:33834209..33834220hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535181
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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