A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169462



Internal ID21313945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141122593..141143891hg38UCSC Ensembl
Outerchr8:141116037..141146731hg38UCSC Ensembl
Innerchr8:142132692..142153990hg19UCSC Ensembl
Outerchr8:142126136..142156830hg19UCSC Ensembl
Innerchr8:142201874..142223172hg18UCSC Ensembl
Outerchr8:142195318..142226012hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3830695
hg1930695
hg1830695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249577
SamplesNGO_25
Known GenesDENND3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169462
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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