A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619480



Internal ID7006354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8164752..8166509hg38UCSC Ensembl
Innerchr9:8164752..8166509hg38UCSC Ensembl
Outerchr9:8164621..8166624hg38UCSC Ensembl
chr9:8164752..8166509hg19UCSC Ensembl
Innerchr9:8164752..8166509hg19UCSC Ensembl
Outerchr9:8164621..8166624hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13394403
SamplesHG00437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619480
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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