A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307350



Internal ID15154298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1850724..1850725hg38UCSC Ensembl
Innerchr9:1850707..1850742hg38UCSC Ensembl
Outerchr9:1850706..1850743hg38UCSC Ensembl
chr9:1850724..1850725hg19UCSC Ensembl
Innerchr9:1850707..1850742hg19UCSC Ensembl
Outerchr9:1850706..1850743hg19UCSC Ensembl
chr9:1840724..1840725hg18UCSC Ensembl
Innerchr9:1840742..1840707hg18UCSC Ensembl
Outerchr9:1840706..1840743hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38287
hg19287
hg18287
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7812327, essv7793024, essv7798876, essv7814246, essv7803991, essv7825728, essv7797236, essv7832829, essv7806152, essv7816474, essv7831980, essv7829756, essv7825974, essv7815915, essv7806934, essv7782212, essv7777819, essv7805602
SamplesNA18502, NA19141, NA18861, NA18508, NA18504, NA19190, NA18870, NA18489, NA19138, NA19137, NA19172, NA18516, NA19114, NA19099, NA19257, NA19225, NA19143, NA18501
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307350
Frequency
Sample Size185
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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