A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303982



Internal ID15150930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87276755..87276756hg38UCSC Ensembl
Innerchr9:87276734..87276777hg38UCSC Ensembl
Outerchr9:87276733..87276778hg38UCSC Ensembl
chr9:89891670..89891671hg19UCSC Ensembl
Innerchr9:89891649..89891692hg19UCSC Ensembl
Outerchr9:89891648..89891693hg19UCSC Ensembl
chr9:89081490..89081491hg18UCSC Ensembl
Innerchr9:89081512..89081469hg18UCSC Ensembl
Outerchr9:89081468..89081513hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386040
hg196040
hg186040
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7805211, essv7819288, essv7772648, essv7811701, essv7833771, essv7801624, essv7782586
SamplesNA12814, NA12155, NA07347, NA11994, NA10847, NA12144, NA12873
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303982
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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