A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5465402



Internal ID8830327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116254742..116258490hg38UCSC Ensembl
Outerchr9:116254585..116258643hg38UCSC Ensembl
Innerchr9:119017021..119020769hg19UCSC Ensembl
Outerchr9:119016864..119020922hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg384059
hg194059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661287
Supporting Variants
SamplesHG00271
Known GenesPAPPA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5465402
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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