A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2490n100



Internal ID20154106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28110984..28203495hg38UCSC Ensembl
chr15:28356130..28448641hg19UCSC Ensembl
chr15:26029725..26122236hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3892512
hg1992512
hg1892512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036445, nsv1042783, nsv1041484, nsv1054402
Samples
Known GenesHERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2490n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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