A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8945303



Internal ID13079268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87276717..87276789hg38UCSC Ensembl
Innerchr9:87276725..87276779hg38UCSC Ensembl
Outerchr9:87276655..87276851hg38UCSC Ensembl
chr9:89891632..89891704hg19UCSC Ensembl
Innerchr9:89891640..89891694hg19UCSC Ensembl
Outerchr9:89891570..89891766hg19UCSC Ensembl
chr9:89081452..89081524hg18UCSC Ensembl
Innerchr9:89081514..89081460hg18UCSC Ensembl
Outerchr9:89081390..89081586hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386040
hg196040
hg186040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3406165
Supporting Variants
SamplesNA07347
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8945303
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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