A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560449



Internal ID333456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100910218..100911759hg38UCSC Ensembl
chr10:102669975..102671516hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560449
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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