A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350061



Internal ID15197043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90087729..90087737hg38UCSC Ensembl
Innerchr6:90087730..90087736hg38UCSC Ensembl
Outerchr6:90087722..90087744hg38UCSC Ensembl
chr6:90797448..90797456hg19UCSC Ensembl
Innerchr6:90797449..90797455hg19UCSC Ensembl
Outerchr6:90797441..90797463hg19UCSC Ensembl
chr6:90854169..90854177hg18UCSC Ensembl
Innerchr6:90854176..90854170hg18UCSC Ensembl
Outerchr6:90854162..90854184hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864625
SamplesNA12005
Known GenesBACH2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350061
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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