A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664633



Internal ID9930738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49519193..49525664hg38UCSC Ensembl
Outerchr15:49519156..49525714hg38UCSC Ensembl
Innerchr15:49811390..49817861hg19UCSC Ensembl
Outerchr15:49811353..49817911hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386559
hg196559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5475204
SamplesNA19904
Known GenesFAM227B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664633
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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