A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621301



Internal ID6661480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103000793..103060898hg38UCSC Ensembl
Innerchr9:103000830..103060861hg38UCSC Ensembl
Outerchr9:103000756..103060935hg38UCSC Ensembl
chr9:105763075..105823180hg19UCSC Ensembl
Innerchr9:105763112..105823143hg19UCSC Ensembl
Outerchr9:105763038..105823217hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3860106
hg1960106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13588155, essv13588156
SamplesHG00375, HG00355
Known GenesCYLC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621301
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer