A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678885



Internal ID9944990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81481387..81489248hg38UCSC Ensembl
Outerchr15:81481350..81489298hg38UCSC Ensembl
Innerchr15:81773728..81781589hg19UCSC Ensembl
Outerchr15:81773691..81781639hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387949
hg197949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6333142, essv5958481
SamplesHG01342, NA12154
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678885
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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