A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2549n100



Internal ID20154165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32990472..33020161hg38UCSC Ensembl
chr15:33282673..33312362hg19UCSC Ensembl
chr15:31069965..31099654hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3829690
hg1929690
hg1829690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047542, nsv1036917
Samples
Known GenesFMN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2549n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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