A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2590n100



Internal ID20154206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44860173..45034007hg38UCSC Ensembl
chr15:45152371..45326205hg19UCSC Ensembl
chr15:42939663..43113497hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38173835
hg19173835
hg18173835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053492, nsv1037941, nsv1054418, nsv1048317
Samples
Known GenesC15orf43, SORD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2590n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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