A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5883704



Internal ID9634578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88405252..88414545hg38UCSC Ensembl
chr9:91020167..91029460hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389294
hg199294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661430
Supporting Variants
SamplesNA19360
Known GenesSPIN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5883704
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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