A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2536n100



Internal ID22788623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31681269..32151995hg38UCSC Ensembl
chr15:31973472..32444196hg19UCSC Ensembl
chr15:29760764..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38470727
hg19470725
hg18470725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040969, nsv1053950, nsv1049618, nsv1044365, nsv1042493, nsv1050178, nsv1048879, nsv1048238, nsv1043340, nsv1039307, nsv1036999, nsv1037698
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2536n100
Frequency
Sample Size11257
Observed Gain33
Observed Loss0
Observed Complex0
Frequencyn/a


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