A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5797448



Internal ID8820567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35391785..35429343hg38UCSC Ensembl
Outerchr15:35391748..35429393hg38UCSC Ensembl
Innerchr15:35683986..35721544hg19UCSC Ensembl
Outerchr15:35683949..35721594hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3837646
hg1937646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672880
Supporting Variants
SamplesHG00262
Known GenesDPH6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5797448
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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