A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621027



Internal ID7007897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89438374..89442180hg38UCSC Ensembl
Innerchr9:89438374..89442180hg38UCSC Ensembl
Outerchr9:89438169..89442393hg38UCSC Ensembl
chr9:92053289..92057095hg19UCSC Ensembl
Innerchr9:92053289..92057095hg19UCSC Ensembl
Outerchr9:92053084..92057308hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549977
SamplesHG04239
Known GenesSEMA4D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621027
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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