A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621564



Internal ID7008432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114938211..114940609hg38UCSC Ensembl
Innerchr9:114938211..114940609hg38UCSC Ensembl
Outerchr9:114938086..114940758hg38UCSC Ensembl
chr9:117700491..117702889hg19UCSC Ensembl
Innerchr9:117700491..117702889hg19UCSC Ensembl
Outerchr9:117700366..117703038hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13607922, essv13607925, essv13607924, essv13607920, essv13607921, essv13607923
SamplesHG02756, HG02981, HG02807, NA19147, HG03049, HG02053
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621564
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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