A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7159n100



Internal ID19017527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28759983..28821165hg38UCSC Ensembl
chr8:28617500..28678682hg19UCSC Ensembl
chr8:28673419..28734601hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3861183
hg1961183
hg1861183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032475, nsv1032142
Samples
Known GenesINTS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7159n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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