A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350032



Internal ID15197014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109177284..109177303hg38UCSC Ensembl
Innerchr6:109177252..109177335hg38UCSC Ensembl
Outerchr6:109177233..109177354hg38UCSC Ensembl
chr6:109498487..109498506hg19UCSC Ensembl
Innerchr6:109498455..109498538hg19UCSC Ensembl
Outerchr6:109498436..109498557hg19UCSC Ensembl
chr6:109605180..109605199hg18UCSC Ensembl
Innerchr6:109605231..109605148hg18UCSC Ensembl
Outerchr6:109605129..109605250hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864633
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350032
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer