A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006802



Internal ID18749333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162203275..162881387hg38UCSC Ensembl
Innerchr3:161921063..162599175hg19UCSC Ensembl
Innerchr3:163403757..164081869hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38678113
hg19678113
hg18678113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607945
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)nsv1006802
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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