A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677144



Internal ID9943249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69077324..69078186hg38UCSC Ensembl
chr15:69369664..69370526hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6247887, essv5970239, essv6468063
SamplesNA19088, NA18963, NA19074
Known GenesMIR548H4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677144
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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