A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2175n100



Internal ID20153791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19811063..22308242hg38UCSC Ensembl
chr15:20016316..22681064hg19UCSC Ensembl
chr15:18276329..20232428hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382497180
hg192664749
hg181956100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039768, nsv1050494, nsv1051797, nsv1055068, nsv1038655
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2175n100
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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