A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6315546



Internal ID9292949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89416349..89418352hg38UCSC Ensembl
Outerchr15:89416192..89418505hg38UCSC Ensembl
Innerchr15:89959580..89961583hg19UCSC Ensembl
Outerchr15:89959423..89961736hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382314
hg192314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659073
Supporting Variants
SamplesNA18628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6315546
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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