A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434194



Internal ID15281148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76521419..76521432hg38UCSC Ensembl
Innerchr9:76521421..76521430hg38UCSC Ensembl
Outerchr9:76521417..76521434hg38UCSC Ensembl
chr9:79136335..79136348hg19UCSC Ensembl
Innerchr9:79136337..79136346hg19UCSC Ensembl
Outerchr9:79136333..79136350hg19UCSC Ensembl
chr9:78326155..78326168hg18UCSC Ensembl
Innerchr9:78326157..78326166hg18UCSC Ensembl
Outerchr9:78326153..78326170hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864934
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434194
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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