A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665863



Internal ID9931968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125481286..125481351hg38UCSC Ensembl
chr9:128243565..128243630hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6220473
SamplesNA18861
Known GenesMAPKAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665863
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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