A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169887



Internal ID21313698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17268401..17293514hg38UCSC Ensembl
Outerchr1:17266911..17296159hg38UCSC Ensembl
Innerchr1:17594896..17620009hg19UCSC Ensembl
Outerchr1:17593406..17622654hg19UCSC Ensembl
Innerchr1:17467483..17492596hg18UCSC Ensembl
Outerchr1:17465993..17495241hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3829249
hg1929249
hg1829249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250548
SamplesMLY_11
Known GenesPADI3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169887
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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