A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3389752



Internal ID15236719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85681710..85681729hg38UCSC Ensembl
Innerchr15:85681706..85681733hg38UCSC Ensembl
Outerchr15:85681687..85681752hg38UCSC Ensembl
chr15:86224941..86224960hg19UCSC Ensembl
Innerchr15:86224937..86224964hg19UCSC Ensembl
Outerchr15:86224918..86224983hg19UCSC Ensembl
chr15:84025945..84025964hg18UCSC Ensembl
Innerchr15:84025968..84025941hg18UCSC Ensembl
Outerchr15:84025922..84025987hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9670025, essv9670014
SamplesNA12815, NA11840
Known GenesAKAP13
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3389752
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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