A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619312



Internal ID7006190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3479988..3508023hg38UCSC Ensembl
Innerchr9:3480000..3508012hg38UCSC Ensembl
Outerchr9:3479977..3508035hg38UCSC Ensembl
chr9:3479988..3508023hg19UCSC Ensembl
Innerchr9:3480000..3508012hg19UCSC Ensembl
Outerchr9:3479977..3508035hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3828036
hg1928036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13380686, essv13380687
SamplesHG01809, HG02397
Known GenesRFX3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619312
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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