A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2535n100



Internal ID22788622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31648339..32387416hg38UCSC Ensembl
chr15:31940542..32679617hg19UCSC Ensembl
chr15:29727834..30466909hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38739078
hg19739076
hg18739076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036910, nsv1048413, nsv1050072, nsv1049073, nsv1042926, nsv1055004, nsv1036271, nsv1051577, nsv1036819, nsv1047365, nsv1052300, nsv1048602, nsv1054979, nsv1042439, nsv1049846, nsv1050183, nsv1049575, nsv1049811, nsv1044429, nsv1048596
Samples
Known GenesCHRNA7, OTUD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2535n100
Frequency
Sample Size11257
Observed Gain37
Observed Loss0
Observed Complex0
Frequencyn/a


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