A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210546



Internal ID22358410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32265161..32268458hg38UCSC Ensembl
chr10:32554089..32557386hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338680, nssv14338679
SamplesNA19238, NA19239
Known GenesEPC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210546
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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