A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228660



Internal ID22370775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71357111..71357297hg38UCSC Ensembl
chr10:73116868..73117054hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354013
SamplesNA19238
Known GenesSLC29A3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228660
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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