A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621198



Internal ID7008067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98024263..98027031hg38UCSC Ensembl
Innerchr9:98024266..98027029hg38UCSC Ensembl
Outerchr9:98024261..98027034hg38UCSC Ensembl
chr9:100786545..100789313hg19UCSC Ensembl
Innerchr9:100786548..100789311hg19UCSC Ensembl
Outerchr9:100786543..100789316hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382769
hg192769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13574293, essv13574306, essv13574289, essv13574290, essv13574298, essv13574294, essv13574301, essv13574300, essv13574296, essv13574303, essv13574302, essv13574304, essv13574292, essv13574291, essv13574305, essv13574299, essv13574295, essv13574297
SamplesNA12286, HG00233, NA20802, HG01518, NA20769, HG01519, HG01495, HG01312, HG01768, NA20832, NA20767, NA20525, HG00155, NA12873, NA20510, HG00280, HG00171, HG01695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621198
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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