A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621086



Internal ID7007956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92660561..92718718hg38UCSC Ensembl
chr9:95422843..95481000hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3858158
hg1958158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559439
SamplesHG02820
Known GenesBICD2, IPPK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621086
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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