A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892652



Internal ID19183472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32097867..32116865hg38UCSC Ensembl
Outerchr15:32097867..32116865hg38UCSC Ensembl
Innerchr15:32390070..32409066hg19UCSC Ensembl
Outerchr15:32390070..32409066hg19UCSC Ensembl
Innerchr15:30177362..30196358hg18UCSC Ensembl
Outerchr15:30177362..30196358hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3818999
hg1918997
hg1818997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783426, essv25801364, essv25800424
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892652
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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