A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv292n100



Internal ID22786379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113313990..113388157hg38UCSC Ensembl
chr1:113856612..113930779hg19UCSC Ensembl
chr1:113658135..113732302hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3874168
hg1974168
hg1874168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009534, nsv1013228, nsv1012143, nsv1005599
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)dgv292n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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