A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009075



Internal ID19098293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109743172..110081182hg38UCSC Ensembl
Innerchr3:109462019..109800029hg19UCSC Ensembl
Innerchr3:110944709..111282719hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38338011
hg19338011
hg18338011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604405
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)nsv1009075
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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