A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621806



Internal ID7008672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128292601..128296131hg38UCSC Ensembl
Innerchr9:128292632..128296101hg38UCSC Ensembl
Outerchr9:128292571..128296162hg38UCSC Ensembl
chr9:131054880..131058410hg19UCSC Ensembl
Innerchr9:131054911..131058380hg19UCSC Ensembl
Outerchr9:131054850..131058441hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383531
hg193531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13622825
SamplesHG03691
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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