A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2660n100



Internal ID20154276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92869548..92932648hg38UCSC Ensembl
chr15:93412778..93475878hg19UCSC Ensembl
chr15:91213782..91276882hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3863101
hg1963101
hg1863101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036560, nsv1047496
Samples
Known GenesCHD2, LOC100507217, MIR3175
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2660n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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