A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015224



Internal ID18757758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28504799..28549099hg38UCSC Ensembl
Innerchr8:28362316..28406616hg19UCSC Ensembl
Innerchr8:28418235..28462535hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3844301
hg1944301
hg1844301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685539
Samples
Known GenesFZD3, MIR4288
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015224
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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