A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5728048



Internal ID8705451
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 StatusS
Merged Variantsesv2671704
Supporting Variants
SamplesNA19469
Known GenesNUSAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5728048
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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