A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169865



Internal ID21313676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4817959..4851939hg38UCSC Ensembl
Outerchr3:4817179..4858918hg38UCSC Ensembl
Innerchr3:4859643..4893623hg19UCSC Ensembl
Outerchr3:4858863..4900602hg19UCSC Ensembl
Innerchr3:4834643..4868623hg18UCSC Ensembl
Outerchr3:4833863..4875602hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3841740
hg1941740
hg1841740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246571
SamplesPML_1
Known GenesITPR1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169865
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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