A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5805083



Internal ID9325072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208477..112210460hg38UCSC Ensembl
chr9:114970757..114972740hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381984
hg191984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666683
Supporting Variants
SamplesNA18519
Known GenesMIR3134
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5805083
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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