A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7864944



Internal ID12970936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87307403..87307436hg38UCSC Ensembl
Innerchr9:87307405..87307434hg38UCSC Ensembl
Outerchr9:87307401..87307438hg38UCSC Ensembl
chr9:89922318..89922351hg19UCSC Ensembl
Innerchr9:89922320..89922349hg19UCSC Ensembl
Outerchr9:89922316..89922353hg19UCSC Ensembl
chr9:89112138..89112171hg18UCSC Ensembl
Innerchr9:89112140..89112169hg18UCSC Ensembl
Outerchr9:89112136..89112173hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3346556
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7864944
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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