A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012854



Internal ID19102071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110614672..110637867hg38UCSC Ensembl
Innerchr3:110333519..110356714hg19UCSC Ensembl
Innerchr3:111816209..111839404hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3823196
hg1923196
hg1823196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604412
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012854
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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