A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13574940



Internal ID3576756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98238011..98238833hg38UCSC Ensembl
Innerchr9:98238011..98238833hg38UCSC Ensembl
Outerchr9:98238011..98238833hg38UCSC Ensembl
chr9:101000293..101001115hg19UCSC Ensembl
Innerchr9:101000293..101001115hg19UCSC Ensembl
Outerchr9:101000293..101001115hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621208
Supporting Variants
SamplesNA19257
Known GenesTBC1D2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13574940
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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