A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620878



Internal ID7007748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81901659..81912474hg38UCSC Ensembl
Innerchr9:81901674..81912459hg38UCSC Ensembl
Outerchr9:81901644..81912489hg38UCSC Ensembl
chr9:84516574..84527389hg19UCSC Ensembl
Innerchr9:84516589..84527374hg19UCSC Ensembl
Outerchr9:84516559..84527404hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3810816
hg1910816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13538747
SamplesHG02383
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620878
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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