A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892653



Internal ID19183473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31736601..32151995hg38UCSC Ensembl
Outerchr15:31726528..32327926hg38UCSC Ensembl
Innerchr15:32028804..32444196hg19UCSC Ensembl
Outerchr15:32018731..32620127hg19UCSC Ensembl
Innerchr15:29816096..30231488hg18UCSC Ensembl
Outerchr15:29806023..30407419hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38601399
hg19601397
hg18601397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789617, essv25792594, essv25790115, essv25788108, essv25787962, essv25792565, essv25791295, essv25789053
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892653
Frequency
Sample Size3017
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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