A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169708



Internal ID21313519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57010486..57020995hg38UCSC Ensembl
Outerchr3:57008286..57022663hg38UCSC Ensembl
Innerchr3:57044514..57055023hg19UCSC Ensembl
Outerchr3:57042314..57056691hg19UCSC Ensembl
Innerchr3:57019554..57030063hg18UCSC Ensembl
Outerchr3:57017354..57031731hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3814378
hg1914378
hg1814378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247500
SamplesNGO_25
Known GenesARHGEF3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169708
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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