A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3449229



Internal ID15296178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20434985..20444683hg38UCSC Ensembl
Innerchr15:20435985..20443683hg38UCSC Ensembl
Outerchr15:20433985..20445683hg38UCSC Ensembl
chr15:20640238..20649936hg19UCSC Ensembl
Innerchr15:20641238..20648936hg19UCSC Ensembl
Outerchr15:20639238..20650936hg19UCSC Ensembl
chr15:18900252..18909950hg18UCSC Ensembl
Innerchr15:18901252..18908950hg18UCSC Ensembl
Outerchr15:18899252..18910950hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg389699
hg199699
hg189699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1356e59
Supporting Variantsessv8689555
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3449229
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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