A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2599n100



Internal ID22788686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53229838..53302552hg38UCSC Ensembl
chr15:53522035..53594749hg19UCSC Ensembl
chr15:51309327..51382041hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3872715
hg1972715
hg1872715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046730, nsv1054695
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)dgv2599n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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