A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169578



Internal ID21313811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95363695..95438699hg38UCSC Ensembl
Outerchr3:95361519..95439499hg38UCSC Ensembl
Innerchr3:95082539..95157543hg19UCSC Ensembl
Outerchr3:95080363..95158343hg19UCSC Ensembl
Innerchr3:96565229..96640233hg18UCSC Ensembl
Outerchr3:96563053..96641033hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3877981
hg1977981
hg1877981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251212
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169578
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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