A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169367



Internal ID21313850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152192479..152320153hg38UCSC Ensembl
Outerchr3:152188516..152323626hg38UCSC Ensembl
Innerchr3:151910268..152037942hg19UCSC Ensembl
Outerchr3:151906305..152041415hg19UCSC Ensembl
Innerchr3:153392958..153520632hg18UCSC Ensembl
Outerchr3:153388995..153524105hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38135111
hg19135111
hg18135111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250714
SamplesPML_1
Known GenesMBNL1, MBNL1-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169367
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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