A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2571n100



Internal ID19012939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34447659..34740872hg38UCSC Ensembl
chr15:34739860..35033073hg19UCSC Ensembl
chr15:32527152..32820365hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38293214
hg19293214
hg18293214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051866, nsv1052277
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2571n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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