A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5558555



Internal ID9506842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75873721..75883655hg38UCSC Ensembl
Outerchr15:75873684..75883705hg38UCSC Ensembl
Innerchr15:76166062..76175996hg19UCSC Ensembl
Outerchr15:76166025..76176046hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3810022
hg1910022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659698
Supporting Variants
SamplesNA18986
Known GenesUBE2Q2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5558555
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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