A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659060



Internal ID9578479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125445832..125447654hg38UCSC Ensembl
chr9:128208111..128209933hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381823
hg191823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6392189
SamplesNA19712
Known GenesMAPKAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659060
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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