A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621400



Internal ID7008269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107564083..107564924hg38UCSC Ensembl
Innerchr9:107564086..107564921hg38UCSC Ensembl
Outerchr9:107564080..107564927hg38UCSC Ensembl
chr9:110326364..110327205hg19UCSC Ensembl
Innerchr9:110326367..110327202hg19UCSC Ensembl
Outerchr9:110326361..110327208hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13594377, essv13594387, essv13594407, essv13594391, essv13594389, essv13594404, essv13594400, essv13594382, essv13594397, essv13594403, essv13594378, essv13594395, essv13594398, essv13594402, essv13594381, essv13594406, essv13594379, essv13594385, essv13594393, essv13594380, essv13594401, essv13594392, essv13594399, essv13594390, essv13594388, essv13594410, essv13594384, essv13594396, essv13594386, essv13594394, essv13594409, essv13594405, essv13594408, essv13594383
SamplesHG03096, HG03175, NA18881, NA18917, HG03515, HG02536, NA19107, HG03086, HG02810, NA18489, HG02562, NA19383, HG02885, NA19239, HG03169, HG01879, HG02666, HG02332, HG02484, NA18909, NA19108, NA19256, NA18517, HG02721, HG01915, NA20351, HG03473, HG02464, HG02971, HG01912, NA19472, HG03063, NA18522, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621400
Frequency
Sample Size2504
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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