A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621057



Internal ID6661238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91254777..91258603hg38UCSC Ensembl
Innerchr9:91254777..91258603hg38UCSC Ensembl
Outerchr9:91254277..91259103hg38UCSC Ensembl
chr9:94017059..94020885hg19UCSC Ensembl
Innerchr9:94017059..94020885hg19UCSC Ensembl
Outerchr9:94016559..94021385hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383827
hg193827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13555526, essv13555527
SamplesNA19376, NA19350
Known GenesAUH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621057
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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