A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3340483



Internal ID15187470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58877162..58877181hg38UCSC Ensembl
Innerchr15:58877158..58877185hg38UCSC Ensembl
Outerchr15:58877139..58877204hg38UCSC Ensembl
chr15:59169361..59169380hg19UCSC Ensembl
Innerchr15:59169357..59169384hg19UCSC Ensembl
Outerchr15:59169338..59169403hg19UCSC Ensembl
chr15:56956653..56956672hg18UCSC Ensembl
Innerchr15:56956676..56956649hg18UCSC Ensembl
Outerchr15:56956630..56956695hg18UCSC Ensembl
Cytoband15q22.1
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 Variantsessv9668914, essv9668903, essv9668892
SamplesNA12814, NA12812, NA12287
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3340483
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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