A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5663n100



Internal ID22791750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50159790..50301693hg38UCSC Ensembl
chr5:49455624..49597527hg19UCSC Ensembl
chr5:49491381..49633284hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38141904
hg19141904
hg18141904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034906, nsv1032046, nsv1021120, nsv1033970, nsv1015794, nsv1034447, nsv1025722
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)dgv5663n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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