A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621482



Internal ID7008351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111100480..111137386hg38UCSC Ensembl
Innerchr9:111100980..111136886hg38UCSC Ensembl
Outerchr9:111099480..111138386hg38UCSC Ensembl
chr9:113862760..113899666hg19UCSC Ensembl
Innerchr9:113863260..113899166hg19UCSC Ensembl
Outerchr9:113861760..113900666hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3836907
hg1936907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13601183
SamplesHG00656
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621482
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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