A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169947



Internal ID21314008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194514736..194557420hg38UCSC Ensembl
Outerchr3:194512809..194564784hg38UCSC Ensembl
Innerchr3:194235465..194278149hg19UCSC Ensembl
Outerchr3:194233538..194285513hg19UCSC Ensembl
Innerchr3:195716754..195759438hg18UCSC Ensembl
Outerchr3:195714827..195766802hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3851976
hg1951976
hg1851976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250984, nssv14241075
SamplesPML_2, PML_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169947
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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