A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559365



Internal ID22428168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43697193..43697193hg38UCSC Ensembl
chr10:44192641..44192641hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344166, nssv14344167
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559365
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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