A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046849



Internal ID19136068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46469221..46489856hg38UCSC Ensembl
Innerchr10:47058780..47080230hg19UCSC Ensembl
Innerchr10:46478786..46500236hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3820636
hg1921451
hg1821451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv805n100
Supporting Variantsnssv3509300
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)nsv1046849
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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