A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620157



Internal ID7007030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28373198..28412495hg38UCSC Ensembl
Innerchr9:28373208..28412485hg38UCSC Ensembl
Outerchr9:28373188..28412505hg38UCSC Ensembl
chr9:28373196..28412493hg19UCSC Ensembl
Innerchr9:28373206..28412483hg19UCSC Ensembl
Outerchr9:28373186..28412503hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3839298
hg1939298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13436621, essv13436622, essv13436623
SamplesHG04206, HG03863, HG03882
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620157
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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