A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621159



Internal ID7008028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96087841..96088976hg38UCSC Ensembl
Innerchr9:96087852..96088965hg38UCSC Ensembl
Outerchr9:96087830..96088987hg38UCSC Ensembl
chr9:98850123..98851258hg19UCSC Ensembl
Innerchr9:98850134..98851247hg19UCSC Ensembl
Outerchr9:98850112..98851269hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13572577, essv13572575, essv13572576, essv13572572, essv13572579, essv13572578, essv13572574, essv13572573, essv13572580
SamplesNA20891, HG04094, HG03944, HG04033, NA20904, HG03775, NA20903, HG01593, NA21133
Known GenesLOC158435
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621159
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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