A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620973



Internal ID7007843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86921131..86928067hg38UCSC Ensembl
Innerchr9:86921188..86928010hg38UCSC Ensembl
Outerchr9:86921074..86928124hg38UCSC Ensembl
chr9:89536046..89542982hg19UCSC Ensembl
Innerchr9:89536103..89542925hg19UCSC Ensembl
Outerchr9:89535989..89543039hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386937
hg196937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1490e214
Supporting Variantsessv13546985
SamplesHG02304
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620973
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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