A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663698



Internal ID9583117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103000925..103061001hg38UCSC Ensembl
Outerchr9:103000891..103061036hg38UCSC Ensembl
Innerchr9:105763207..105823283hg19UCSC Ensembl
Outerchr9:105763173..105823318hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3860146
hg1960146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1363e199
Supporting Variantsessv6396710
SamplesHG00375
Known GenesCYLC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663698
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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