A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657927



Internal ID9924032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4202243..4257633hg38UCSC Ensembl
Outerchr9:4202206..4257683hg38UCSC Ensembl
Innerchr9:4202243..4257633hg19UCSC Ensembl
Outerchr9:4202206..4257683hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3855478
hg1955478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6210745
SamplesNA19313
Known GenesGLIS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657927
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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