A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5860773



Internal ID8838176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90841444..90842179hg38UCSC Ensembl
chr9:93603726..93604461hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669899
Supporting Variants
SamplesNA20808
Known GenesSYK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5860773
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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