A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678654



Internal ID9944759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74379745..74380468hg38UCSC Ensembl
Outerchr15:74379708..74380518hg38UCSC Ensembl
Innerchr15:74672086..74672809hg19UCSC Ensembl
Outerchr15:74672049..74672859hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6534679
SamplesHG00338
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678654
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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