A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3392528



Internal ID15239493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91409302..91409344hg38UCSC Ensembl
Innerchr15:91409316..91409327hg38UCSC Ensembl
Outerchr15:91409277..91409369hg38UCSC Ensembl
chr15:91952532..91952574hg19UCSC Ensembl
Innerchr15:91952546..91952557hg19UCSC Ensembl
Outerchr15:91952507..91952599hg19UCSC Ensembl
chr15:89753536..89753578hg18UCSC Ensembl
Innerchr15:89753561..89753550hg18UCSC Ensembl
Outerchr15:89753511..89753603hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38262
hg19262
hg18262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8969340, essv8969342, essv8969341, essv8969343
SamplesNA18861, NA18507, NA18498, NA18912
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3392528
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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