A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528853



Internal ID22398245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52643568..52643756hg38UCSC Ensembl
chr10:54403328..54403516hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347158, nssv14346539, nssv14347157, nssv14346540, nssv14347156
SamplesNA19238, NA19239, HG00731, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528853
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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