A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2532n100



Internal ID19012900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30628409..30753286hg38UCSC Ensembl
chr15:30920612..31045489hg19UCSC Ensembl
chr15:28707904..28832781hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38124878
hg19124878
hg18124878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051214, nsv1046245, nsv1043532
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2532n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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