A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658555



Internal ID9924660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123213508..123219979hg38UCSC Ensembl
Outerchr9:123213471..123220029hg38UCSC Ensembl
Innerchr9:125975787..125982258hg19UCSC Ensembl
Outerchr9:125975750..125982308hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386559
hg196559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6243728
SamplesHG00231
Known GenesSTRBP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658555
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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