A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169721



Internal ID21313532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13136166..13148173hg38UCSC Ensembl
Outerchr3:13131212..13151685hg38UCSC Ensembl
Innerchr3:13177666..13189673hg19UCSC Ensembl
Outerchr3:13172712..13193185hg19UCSC Ensembl
Innerchr3:13152666..13164673hg18UCSC Ensembl
Outerchr3:13147712..13168185hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3820474
hg1920474
hg1820474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252300
SamplesNGO_23
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169721
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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