A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6247887



Internal ID9556302
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 StatusS
Merged Variantsesv2677144
Supporting Variants
SamplesNA19088
Known GenesMIR548H4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6247887
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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