A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169406



Internal ID21313889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100595356..100602358hg38UCSC Ensembl
Outerchr10:100593790..100604247hg38UCSC Ensembl
Innerchr10:102355113..102362115hg19UCSC Ensembl
Outerchr10:102353547..102364004hg19UCSC Ensembl
Innerchr10:102345103..102352105hg18UCSC Ensembl
Outerchr10:102343537..102353994hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3810458
hg1910458
hg1810458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243392
SamplesNGO_22
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169406
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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