A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5797563



Internal ID8865068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132881708..132882507hg38UCSC Ensembl
chr9:135757095..135757894hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671227
Supporting Variants
SamplesHG00320
Known GenesC9orf9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5797563
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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