A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214441



Internal ID22361100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28685643..28691683hg38UCSC Ensembl
chr10:28974572..28980612hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386041
hg196041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337376
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214441
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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