A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6224839



Internal ID9202242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91298923..91302133hg38UCSC Ensembl
Outerchr9:91298886..91302183hg38UCSC Ensembl
Innerchr9:94061205..94064415hg19UCSC Ensembl
Outerchr9:94061168..94064465hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676899
Supporting Variants
SamplesNA19472
Known GenesAUH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6224839
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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