A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304694



Internal ID15151642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90020576..90020577hg38UCSC Ensembl
Innerchr6:90020542..90020611hg38UCSC Ensembl
Outerchr6:90020541..90020612hg38UCSC Ensembl
chr6:90730295..90730296hg19UCSC Ensembl
Innerchr6:90730261..90730330hg19UCSC Ensembl
Outerchr6:90730260..90730331hg19UCSC Ensembl
chr6:90787016..90787017hg18UCSC Ensembl
Innerchr6:90787051..90786982hg18UCSC Ensembl
Outerchr6:90786981..90787052hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38237
hg19237
hg18237
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7761522, essv7746017, essv7761282, essv7751542, essv7759508, essv7742906, essv7761013, essv7757081, essv7752916, essv7754354
SamplesNA11829, NA18507, NA11920, NA12287, NA19238, NA12003, NA18499, NA19240, NA18505, NA12154
Known GenesBACH2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304694
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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