A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008940



Internal ID18751471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93800622..93864299hg38UCSC Ensembl
Innerchr3:93519466..93583143hg19UCSC Ensembl
Innerchr3:95002156..95065833hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3863678
hg1963678
hg1863678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4813n100
Supporting Variantsnssv3603292, nssv3603295, nssv3603294, nssv3603293
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)nsv1008940
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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