A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6080141



Internal ID9567978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73452055..73465339hg38UCSC Ensembl
chr9:76066971..76080255hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3813285
hg1913285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665701
Supporting Variants
SamplesNA19116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6080141
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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