A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306394



Internal ID15153342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88230884..88230885hg38UCSC Ensembl
Innerchr9:88230867..88230902hg38UCSC Ensembl
Outerchr9:88230866..88230903hg38UCSC Ensembl
chr9:90845799..90845800hg19UCSC Ensembl
Innerchr9:90845782..90845817hg19UCSC Ensembl
Outerchr9:90845781..90845818hg19UCSC Ensembl
chr9:90035619..90035620hg18UCSC Ensembl
Innerchr9:90035637..90035602hg18UCSC Ensembl
Outerchr9:90035601..90035638hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38141
hg19141
hg18141
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7795983, essv7809831, essv7819913, essv7805547, essv7808877, essv7807940, essv7797329, essv7833017, essv7805028, essv7787752, essv7805682, essv7782890, essv7770432, essv7771013, essv7789141
SamplesNA11920, NA12155, NA18550, NA11992, NA12287, NA12828, NA18605, NA12872, NA18566, NA18573, NA12249, NA19099, NA19257, NA18858, NA12716
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306394
Frequency
Sample Size185
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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