A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169841



Internal ID21313652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42822218..42993457hg38UCSC Ensembl
Outerchr21:42816587..42997564hg38UCSC Ensembl
Innerchr21:44242328..44413567hg19UCSC Ensembl
Outerchr21:44236697..44417674hg19UCSC Ensembl
Innerchr21:43115397..43286636hg18UCSC Ensembl
Outerchr21:43109766..43290743hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38180978
hg19180978
hg18180978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244440, nssv14251876, nssv14248891, nssv14246781
SamplesNGO_3, NGO_10, NGO_30, SNI_5
Known GenesNDUFV3, PKNOX1, WDR4
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169841
Frequency
Sample Size93
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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