A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5511n100



Internal ID22791598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15520..63270hg38UCSC Ensembl
chr5:15520..63385hg19UCSC Ensembl
chr5:68520..116385hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3847751
hg1947866
hg1847866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023317, nsv1021895, nsv1028147
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)dgv5511n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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