A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666375



Internal ID9585794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105765185..105777641hg38UCSC Ensembl
Outerchr9:105764814..105778011hg38UCSC Ensembl
Innerchr9:108527466..108539922hg19UCSC Ensembl
Outerchr9:108527095..108540292hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3813198
hg1913198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5948576, essv6119178
SamplesNA19004, NA18984
Known GenesTMEM38B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666375
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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