A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670662



Internal ID9936767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111261806..111273989hg38UCSC Ensembl
Outerchr9:111261648..111274142hg38UCSC Ensembl
Innerchr9:114024086..114036269hg19UCSC Ensembl
Outerchr9:114023928..114036422hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3812495
hg1912495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6257569
SamplesNA19835
Known GenesMIR7702
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670662
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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