A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8945484



Internal ID12852594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91296197..91296203hg38UCSC Ensembl
Innerchr9:91296189..91296209hg38UCSC Ensembl
Outerchr9:91296185..91296215hg38UCSC Ensembl
chr9:94058479..94058485hg19UCSC Ensembl
Innerchr9:94058471..94058491hg19UCSC Ensembl
Outerchr9:94058467..94058497hg19UCSC Ensembl
chr9:93098300..93098306hg18UCSC Ensembl
Innerchr9:93098312..93098292hg18UCSC Ensembl
Outerchr9:93098288..93098318hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3337917
Supporting Variants
SamplesNA11919
Known GenesAUH
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8945484
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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