A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619392



Internal ID7006270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6034482..6039827hg38UCSC Ensembl
Innerchr9:6034482..6039827hg38UCSC Ensembl
Outerchr9:6034351..6039978hg38UCSC Ensembl
chr9:6034482..6039827hg19UCSC Ensembl
Innerchr9:6034482..6039827hg19UCSC Ensembl
Outerchr9:6034351..6039978hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385346
hg195346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13385778
SamplesNA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619392
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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