A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666509



Internal ID9585928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91801066..91803780hg38UCSC Ensembl
Outerchr9:91801029..91803830hg38UCSC Ensembl
Innerchr9:94563348..94566062hg19UCSC Ensembl
Outerchr9:94563311..94566112hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5552118
SamplesNA19099
Known GenesROR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666509
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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