A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662785



Internal ID9928890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125596425..125603816hg38UCSC Ensembl
Outerchr9:125596268..125603969hg38UCSC Ensembl
Innerchr9:128358704..128366095hg19UCSC Ensembl
Outerchr9:128358547..128366248hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387702
hg197702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5504658
SamplesHG00137
Known GenesMAPKAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662785
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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