A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620557



Internal ID7007427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69371015..69372269hg38UCSC Ensembl
Innerchr9:69371245..69372039hg38UCSC Ensembl
Outerchr9:69370785..69372499hg38UCSC Ensembl
chr9:71985931..71987185hg19UCSC Ensembl
Innerchr9:71986161..71986955hg19UCSC Ensembl
Outerchr9:71985701..71987415hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13511308
SamplesNA19064
Known GenesFAM189A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620557
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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