A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664946



Internal ID9931051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86985775..86986588hg38UCSC Ensembl
chr15:87529006..87529819hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6056667, essv6258556
SamplesNA19446, NA19445
Known GenesAGBL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664946
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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