A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999942



Internal ID18812792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71131662..71736899hg38UCSC Ensembl
Innerchr3:71180813..71786050hg19UCSC Ensembl
Innerchr3:71263503..71868740hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38605238
hg19605238
hg18605238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594155
Samples
Known GenesEIF4E3, FOXP1, MIR1284
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999942
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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