A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6306856



Internal ID9284259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129763787..129768093hg38UCSC Ensembl
Outerchr9:129763416..129768463hg38UCSC Ensembl
Innerchr9:132526066..132530372hg19UCSC Ensembl
Outerchr9:132525695..132530742hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385048
hg195048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658845
Supporting Variants
SamplesNA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6306856
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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