A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676294



Internal ID9942399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87259662..87264656hg38UCSC Ensembl
Outerchr9:87259625..87264706hg38UCSC Ensembl
Innerchr9:89874577..89879571hg19UCSC Ensembl
Outerchr9:89874540..89879621hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385082
hg195082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6240365
SamplesNA19723
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676294
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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