A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669530



Internal ID9935635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69023704..69025355hg38UCSC Ensembl
chr15:69316044..69317695hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6086357, essv6162642
SamplesNA18520, NA18910
Known GenesMIR548H4, NOX5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669530
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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