A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892743



Internal ID19183563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99456357..99482510hg38UCSC Ensembl
Outerchr15:99456357..99482510hg38UCSC Ensembl
Innerchr15:99996562..100022715hg19UCSC Ensembl
Outerchr15:99996562..100022715hg19UCSC Ensembl
Innerchr15:97814085..97840238hg18UCSC Ensembl
Outerchr15:97814085..97840238hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3826154
hg1926154
hg1826154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792867
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892743
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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