A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008569



Internal ID19097786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98218324..98264273hg38UCSC Ensembl
Innerchr3:97937168..97983117hg19UCSC Ensembl
Innerchr3:99419858..99465807hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3845950
hg1945950
hg1845950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4818n100
Supporting Variantsnssv3603322
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)nsv1008569
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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