A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033747



Internal ID19122968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104419773..104481736hg38UCSC Ensembl
Innerchr6:104867648..104929611hg19UCSC Ensembl
Innerchr6:104974341..105036304hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3861964
hg1961964
hg1861964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653503
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)nsv1033747
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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