A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5449787



Internal ID8427190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91776717..91777646hg38UCSC Ensembl
Outerchr9:91776680..91777696hg38UCSC Ensembl
Innerchr9:94538999..94539928hg19UCSC Ensembl
Outerchr9:94538962..94539978hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674278
Supporting Variants
SamplesHG01101
Known GenesROR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5449787
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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