A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6553361



Internal ID9530764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76782489..76783239hg38UCSC Ensembl
chr9:79397405..79398155hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663601
Supporting Variants
SamplesNA19007
Known GenesPCA3, PRUNE2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6553361
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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