A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307811



Internal ID15154759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14877435..14877436hg38UCSC Ensembl
Innerchr9:14877418..14877453hg38UCSC Ensembl
Outerchr9:14877417..14877454hg38UCSC Ensembl
chr9:14877433..14877434hg19UCSC Ensembl
Innerchr9:14877416..14877451hg19UCSC Ensembl
Outerchr9:14877415..14877452hg19UCSC Ensembl
chr9:14867433..14867434hg18UCSC Ensembl
Innerchr9:14867451..14867416hg18UCSC Ensembl
Outerchr9:14867415..14867452hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7801634, essv7780959, essv7799560, essv7820656, essv7812269, essv7805525, essv7798083, essv7796987, essv7777991, essv7806021, essv7770994, essv7778822, essv7833524, essv7819168, essv7787507, essv7784062, essv7807065, essv7813397, essv7795673, essv7835398, essv7825617, essv7785543
SamplesNA18502, NA11830, NA18861, NA10851, NA12414, NA12751, NA18870, NA07347, NA12761, NA19239, NA10847, NA19114, NA11919, NA12249, NA19257, NA18858, NA12716, NA07051, NA18501, NA12749, NA12006, NA18522
Known GenesFREM1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307811
Frequency
Sample Size185
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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