A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673810



Internal ID9939915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91532958..91534427hg38UCSC Ensembl
Outerchr9:91532801..91534580hg38UCSC Ensembl
Innerchr9:94295240..94296709hg19UCSC Ensembl
Outerchr9:94295083..94296862hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5772425
SamplesNA18628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673810
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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