A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169896



Internal ID21313707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33366168..33437678hg38UCSC Ensembl
Outerchr21:33362204..33443487hg38UCSC Ensembl
Innerchr21:34738474..34809985hg19UCSC Ensembl
Outerchr21:34734510..34815794hg19UCSC Ensembl
Innerchr21:33660344..33731855hg18UCSC Ensembl
Outerchr21:33656380..33737664hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3881284
hg1981285
hg1881285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250270
SamplesPML_1
Known GenesIFNGR2, TMEM50B
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169896
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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