A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656856



Internal ID9922961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89005743..89008316hg38UCSC Ensembl
Outerchr15:89005706..89008366hg38UCSC Ensembl
Innerchr15:89548974..89551547hg19UCSC Ensembl
Outerchr15:89548937..89551597hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382661
hg192661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5528518, essv6085273, essv5903480
SamplesNA19819, NA19130, NA18933
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656856
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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