A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5778547



Internal ID9644085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52804319..52806425hg38UCSC Ensembl
Outerchr15:52803948..52806795hg38UCSC Ensembl
Innerchr15:53096516..53098622hg19UCSC Ensembl
Outerchr15:53096145..53098992hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674891
Supporting Variants
SamplesNA19376
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5778547
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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