A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892638



Internal ID19183458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24771381..24801829hg38UCSC Ensembl
Outerchr15:24771381..24801829hg38UCSC Ensembl
Innerchr15:25016528..25046976hg19UCSC Ensembl
Outerchr15:25016528..25046976hg19UCSC Ensembl
Innerchr15:22567621..22598069hg18UCSC Ensembl
Outerchr15:22567621..22598069hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3830449
hg1930449
hg1830449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792623
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892638
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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