A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169928



Internal ID21313989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68852888..68856761hg38UCSC Ensembl
Outerchr10:68851487..68858935hg38UCSC Ensembl
Innerchr10:70612644..70616517hg19UCSC Ensembl
Outerchr10:70611243..70618691hg19UCSC Ensembl
Innerchr10:70282650..70286523hg18UCSC Ensembl
Outerchr10:70281249..70288697hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387449
hg197449
hg187449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246569
SamplesNGO_14
Known GenesSTOX1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169928
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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