A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5418168



Internal ID9583483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84641053..84641241hg38UCSC Ensembl
chr15:85184284..85184472hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657745
Supporting Variants
SamplesNA19172
Known GenesSCAND2P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5418168
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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