A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671704



Internal ID9591123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41377762..41378495hg38UCSC Ensembl
Outerchr15:41377725..41378545hg38UCSC Ensembl
Innerchr15:41669960..41670693hg19UCSC Ensembl
Outerchr15:41669923..41670743hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5728048, essv6410981
SamplesNA19469, NA19448
Known GenesNUSAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671704
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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