A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666630



Internal ID9586049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91073348..91073431hg38UCSC Ensembl
chr9:93835630..93835713hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6232116, essv5663180, essv5716239, essv6493582, essv5667942, essv6116353, essv6385123
SamplesNA19093, NA19379, NA19428, NA19398, NA18504, NA19394, NA19381
Known GenesLOC100129316
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666630
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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