A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662525



Internal ID9928630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93172163..93174273hg38UCSC Ensembl
Outerchr9:93172126..93174323hg38UCSC Ensembl
Innerchr9:95934445..95936555hg19UCSC Ensembl
Outerchr9:95934408..95936605hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382198
hg192198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5636595
SamplesNA11932
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662525
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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