A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892639



Internal ID19183459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27174705..27237623hg38UCSC Ensembl
Outerchr15:27174705..27237623hg38UCSC Ensembl
Innerchr15:27419852..27482770hg19UCSC Ensembl
Outerchr15:27419852..27482770hg19UCSC Ensembl
Innerchr15:25002598..25065516hg18UCSC Ensembl
Outerchr15:25002598..25065516hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3862919
hg1962919
hg1862919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789085
Samples
Known GenesGABRG3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892639
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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