A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5852407



Internal ID8936922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34935437..34938736hg38UCSC Ensembl
Outerchr9:34935400..34938786hg38UCSC Ensembl
Innerchr9:34935434..34938733hg19UCSC Ensembl
Outerchr9:34935397..34938783hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669806
Supporting Variants
SamplesHG00463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5852407
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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